Isolated nucleic acid molecules encoding human enzyme proteins, and uses thereof

ABSTRACT

The present invention provides amino acid sequences of peptides that are encoded by genes within the human genome, the enzyme peptides of the present invention. The present invention specifically provides isolated peptide and nucleic acid molecules, methods of identifying orthologs and paralogs of the enzyme peptides, and methods of identifying modulators of the enzyme peptides.

FIELD OF THE INVENTION

The present invention is in the field of enzyme proteins that are related to the helicase subfamily, recombinant DNA molecules, and protein production. The present invention specifically provides novel peptides and proteins that effect protein phosphorylation and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.

BACKGROUND OF THE INVENTION

Many human enzymes serve as targets for the action of pharmaceutically active compounds. Several classes of human enzymes that serve as such targets include helicase, steroid esterase and sulfatase, convertase, synthase, dehydrogenase, monoxygenase, transferase, kinase, glutanase, decarboxylase, isomerase and reductase. It is therefore important in developing new pharmaceutical compounds to identify target enzyme proteins that can be put into high-throughput screening formats. The present invention advances the state of the art by providing novel human drug target enzymes related to the helicase subfamily.

Helicases

The novel human enzyme, and encoding gene is similar to the RNA helicase HDB protein, also known as the DICE1 (“deleted in cancer 1”) protein.

DICE1 is a candidate tumor suppressor gene, particularly in non-small cell lung carcinomas, and carcinomas of the head and neck, breast, ovary, prostate, as well as other carcinomas. DICE1 is expressed in a wide variety of adult and fetal tissues and is highly conserved in evolution, it's expression is down-regulated or abolished in carcinomas, and it is located in a chromosomal region associated with tumor suppression and loss of heterozygosity. DICE1 shares 92.9% amino acid sequence identity with the carboxy-terminal half of mouse EGF repeat transmembrane protein DB-1, a protein that limits mitogenic response to insulin-like growth factor 1 and likely plays a role in anchorage-dependent growth (Wieland et al, Oncogene 18: 4530-4537, 1999).

Therefore, novel human helicase proteins/genes may be particularly useful in the diagnosis, prevention, and/or treatment of carcinomas.

Enzyme proteins, particularly members of the helicase subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of enzyme proteins. The present invention advances the state of the art by providing previously unidentified human enzyme proteins, and the polynucleotides encoding them, that have homology to members of the helicase subfamily. These novel compositions are useful in the diagnosis, prevention and treatment of biological processes associated with human diseases.

SUMMARY OF THE INVENTION

The present invention is based in part on the identification of amino acid sequences of human enzyme peptides and proteins that are related to the helicase subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate enzyme activity in cells and tissues that express the enzyme. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain.

DESCRIPTION OF THE FIGURE SHEETS

FIG. 1 provides the nucleotide sequence of a cDNA molecule that encodes the enzyme protein of the present invention. (SEQ ID NO:1) In addition, structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain.

FIG. 2 provides the predicted amino acid sequence of the enzyme of the present invention. (SEQ ID NO:2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.

FIG. 3 provides genomic sequences that span the gene encoding the enzyme protein of the present invention. (SEQ ID NO:3) In addition structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.

DETAILED DESCRIPTION OF THE INVENTION General Description

The present invention is based on the sequencing of the human genome. During the sequencing and assembly of the human genome, analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a enzyme protein or part of a enzyme protein and are related to the helicase subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized. Based on this analysis, the present invention provides amino acid sequences of human enzyme peptides and proteins that are related to the helicase subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these enzyme peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the enzyme of the present invention.

In addition to being previously unknown, the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known enzyme proteins of the helicase subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene. Some of the more specific features of the peptides of the present invention, and the uses thereof, are described herein, particularly in the Background of the Invention and in the annotation provided in the Figures, and/or are known within the art for each of the known helicase family or subfamily of enzyme proteins.

Specific Embodiments

Peptide Molecules

The present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the enzyme family of proteins and are related to the helicase subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3). The peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the enzyme peptides of the present invention, enzyme peptides, or peptides/proteins of the present invention.

The present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the enzyme peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.

As used herein, a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals. The peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).

In some uses, “substantially free of cellular material” includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins. When the peptide is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.

The language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the enzyme peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.

The isolated enzyme peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. For example, a nucleic acid molecule encoding the enzyme peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell. The protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.

Accordingly, the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). The amino acid sequence of such a protein is provided in FIG. 2. A protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.

The present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.

The present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids. The preferred classes of proteins that are comprised of the enzyme peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.

The enzyme peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins. Such chimeric and fusion proteins comprise a enzyme peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the enzyme peptide. “Operatively linked” indicates that the enzyme peptide and the heterologous protein are fused in-frame. The heterologous protein can be fused to the N-terminus or C-terminus of the enzyme peptide.

In some uses, the fusion protein does not affect the activity of the enzyme peptide per se. For example, the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions. Such fusion proteins, particularly poly-His fusions, can facilitate the purification of recombinant enzyme peptide. In certain host cells (e.g., mammalian host cells), expression and/or secretion of a protein can be increased by using a heterologous signal sequence.

A chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al., Current Protocols in Molecular Biology, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein). A enzyme peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the enzyme peptide.

As mentioned above, the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides. Such variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.

Such variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the enzyme peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.

To determine the percent identity of two amino acid sequences or two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In a preferred embodiment, at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.

The comparison of sequences and determination of percent identity and similarity between two sequences can be accomplished using a mathematical algorithm. (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part 1, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991). In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.

The nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (J. Mol. Biol. 215:403-10 (1990)). BLAST nucleotide searches can be performed with the NBLAST program, score=100, wordlength=12 to obtain nucleotide sequences homologous to the nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score=50, wordlength=3 to obtain amino acid sequences homologous to the proteins of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (Nucleic Acids Res. 25(17):3389-3402 (1997)). When utilizing BLAST and gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used.

Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the enzyme peptides of the present invention as well as being encoded by the same genetic locus as the enzyme peptide provided herein. The gene encoding the novel enzyme of the present invention is located on a genome component that has been mapped to human chromosome X (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.

Allelic variants of a enzyme peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the enzyme peptide as well as being encoded by the same genetic locus as the enzyme peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. The gene encoding the novel enzyme of the present invention is located on a genome component that has been mapped to human chromosome X (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data. As used herein, two proteins (or a region of the proteins) have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous. A significantly homologous amino acid sequence, according to the present invention, will be encoded by a nucleic acid sequence that will hybridize to a enzyme peptide encoding nucleic acid molecule under stringent conditions as more fully described below.

Paralogs of a enzyme peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the enzyme peptide, as being encoded by a gene from humans, and as having similar activity or function. Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain. Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a enzyme peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.

Orthologs of a enzyme peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the enzyme peptide as well as being encoded by a gene from another organism. Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents. Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a enzyme peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins.

Non-naturally occurring variants of the enzyme peptides of the present invention can readily be generated using recombinant techniques. Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the enzyme peptide. For example, one class of substitutions are conserved amino acid substitution. Such substitutions are those that substitute a given amino acid in a enzyme peptide by another amino acid of like characteristics. Typically seen as conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr. Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al., Science 247:1306-1310 (1990).

Variant enzyme peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to phosphorylate substrate, ability to mediate signaling, etc. Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions. FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions. Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.

Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.

Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al., Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as enzyme activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).

The present invention further provides fragments of the enzyme peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2. The fragments to which the invention pertains, however, are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.

As used herein, a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a enzyme peptide. Such fragments can be chosen based on the ability to retain one or more of the biological activities of the enzyme peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen. Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length. Such fragments will typically comprise a domain or motif of the enzyme peptide, e.g., active site, a transmembrane domain or a substrate-binding domain. Further, possible fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures. Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.

Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in enzyme peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).

Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.

Such modifications are well known to those of skill in the art and have been described in great detail in the scientific literature. Several particularly common modifications, glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutamic acid residues, hydroxylation and ADP-ribosylation, for instance, are described in most basic texts, such as Proteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993). Many detailed reviews are available on this subject, such as by Wold, F., Posttranslational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York 1-12 (1983); Seifter et al. (Meth. Enzymol. 182: 626-646 (1990)) and Rattan et al. (Ann. N.Y. Acad. Sci. 663:48-62 (1992)).

Accordingly, the enzyme peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature enzyme peptide is fused with another compound, such as a compound to increase the half-life of the enzyme peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature enzyme peptide, such as a leader or secretory sequence or a sequence for purification of the mature enzyme peptide or a pro-protein sequence.

Protein/Peptide Uses

The proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state). Where the protein binds or potentially binds to another protein or ligand (such as, for example, in a enzyme-effector protein interaction or enzyme-ligand interaction), the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.

Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.

The potential uses of the peptides of the present invention are based primarily on the source of the protein as well as the class/action of the protein. For example, enzymes isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the enzyme. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain. A large percentage of pharmaceutical agents are being developed that modulate the activity of enzyme proteins, particularly members of the helicase subfamily (see Background of the Invention). The structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. Such uses can readily be determined using the information provided herein, that which is known in the art, and routine experimentation.

The proteins of the present invention (including variants and fragments that may have been disclosed prior to the present invention) are useful for biological assays related to enzymes that are related to members of the helicase subfamily. Such assays involve any of the known enzyme functions or activities or properties useful for diagnosis and treatment of enzyme-related conditions that are specific for the subfamily of enzymes that the one of the present invention belongs to, particularly in cells and tissues that express the enzyme. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain.

The proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems. Cell-based systems can be native, i.e., cells that normally express the enzyme, as a biopsy or expanded in cell culture. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. In an alternate embodiment, cell-based assays involve recombinant host cells expressing the enzyme protein.

The polypeptides can be used to identify compounds that modulate enzyme activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the enzyme. Both the enzymes of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the enzyme. These compounds can be further screened against a functional enzyme to determine the effect of the compound on the enzyme activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the enzyme to a desired degree.

Further, the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the enzyme protein and a molecule that normally interacts with the enzyme protein, e.g. a substrate or a component of the signal pathway that the enzyme protein normally interacts (for example, another enzyme). Such assays typically include the steps of combining the enzyme protein with a candidate compound under conditions that allow the enzyme protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the enzyme protein and the target, such as any of the associated effects of signal transduction such as protein phosphorylation, cAMP turnover, and adenylate cyclase activation, etc.

Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L-configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′)₂, Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules (e.g., molecules obtained from combinatorial and natural product libraries).

One candidate compound is a soluble fragment of the receptor that competes for substrate binding. Other candidate compounds include mutant enzymes or appropriate fragments containing mutations that affect enzyme function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.

The invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) enzyme activity. The assays typically involve an assay of events in the signal transduction pathway that indicate enzyme activity. Thus, the phosphorylation of a substrate, activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the enzyme protein dependent signal cascade can be assayed.

Any of the biological or biochemical functions mediated by the enzyme can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the enzyme can be assayed. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain.

Binding and/or activating compounds can also be screened by using chimeric enzyme proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions. For example, a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native enzyme. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the enzyme is derived.

The proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the enzyme (e.g. binding partners and/or ligands). Thus, a compound is exposed to a enzyme polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide. Soluble enzyme polypeptide is also added to the mixture. If the test compound interacts with the soluble enzyme polypeptide, it decreases the amount of complex formed or activity from the enzyme target. This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the enzyme. Thus, the soluble polypeptide that competes with the target enzyme region is designed to contain peptide sequences corresponding to the region of interest.

To perform cell free drug screening assays, it is sometimes desirable to immobilize either the enzyme protein, or fragment, or its target molecule to facilitate separation of complexes from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay.

Techniques for immobilizing proteins on matrices can be used in the drug screening assays. In one embodiment, a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix. For example, glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtitre plates, which are then combined with the cell lysates (e.g., ³⁵S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated. Alternatively, the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of enzyme-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques. For example, either the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art. Alternatively, antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation. Preparations of a enzyme-binding protein and a candidate compound are incubated in the enzyme protein-presenting wells and the amount of complex trapped in the well can be quantitated. Methods for detecting such complexes, in addition to those described above for the GST-immobilized complexes, include immunodetection of complexes using antibodies reactive with the enzyme protein target molecule, or which are reactive with enzyme protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.

Agents that modulate one of the enzymes of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.

Modulators of enzyme protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the enzyme pathway, by treating cells or tissues that express the enzyme. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. These methods of treatment include the steps of administering a modulator of enzyme activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.

In yet another aspect of the invention, the enzyme proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al. (1993) Cell 72:223-232; Madura et al. (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al. (1993) Oncogene 8:1693-1696; and Brent WO94/10300), to identify other proteins, which bind to or interact with the enzyme and are involved in enzyme activity. Such enzyme-binding proteins are also likely to be involved in the propagation of signals by the enzyme proteins or enzyme targets as, for example, downstream elements of a enzyme-mediated signaling pathway. Alternatively, such enzyme-binding proteins are likely to be enzyme inhibitors.

The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for a enzyme protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor. If the “bait” and the “prey” proteins are able to interact, in vivo, forming a enzyme-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the enzyme protein.

This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e.g., a enzyme-modulating agent, an antisense enzyme nucleic acid molecule, a enzyme-specific antibody, or a enzyme-binding partner) can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent. Alternatively, an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.

The enzyme proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. The method involves contacting a biological sample with a compound capable of interacting with the enzyme protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein. A biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.

The peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs. Thus, the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification. Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered enzyme activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

In vitro techniques for detection of peptide include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent. Alternatively, the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.

The peptides are also useful in pharmacogenomic analysis. Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. (Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. (Clin. Chem. 43(2):254-266 (1997)). The clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism. Thus, the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound. Further, the activity of drug metabolizing enzymes effects both the intensity and duration of drug action. Thus, the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype. The discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the enzyme protein in which one or more of the enzyme function in one population is different from those in another population. The peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality. Thus, in a ligand-based treatment, polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and enzyme activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism. As an alternative to genotyping, specific polymorphic peptides could be identified.

The peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. Accordingly, methods for treatment include the use of the enzyme protein or fragments.

Antibodies

The invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof. As used herein, an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins. An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.

As used herein, an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge. The antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′)₂, and Fv fragments.

Many methods are known for generating and/or identifying antibodies to a given target peptide. Several such methods are described by Harlow, Antibodies, Cold Spring Harbor Press, (1989).

In general, to generate antibodies, an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse. The full-length protein, an antigenic peptide fragment or a fusion protein can be used. Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.

Antibodies are preferably prepared from regions or discrete fragments of the enzyme proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or enzyme/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.

An antigenic fragment will typically comprise at least 8 contiguous amino acid residues. The antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues. Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).

Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include ¹²⁵I, ¹³¹I, ³⁵S or ³H.

Antibody Uses

The antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation. The antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells. In addition, such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain. Further, such antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.

Further, the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function. When a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form, the antibody can be prepared against the normal protein. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.

The antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. The diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.

Additionally, antibodies are useful in pharmacogenomic analysis. Thus, antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities. The antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.

The antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.

The antibodies are also useful for inhibiting protein function, for example, blocking the binding of the enzyme peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function. An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity. Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.

The invention also encompasses kits for using antibodies to detect the presence of a protein in a biological sample. The kit can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use. Such a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nuleic acid arrays and similar methods have been developed for antibody arrays.

Nucleic Acid Molecules

The present invention further provides isolated nucleic acid molecules that encode a enzyme peptide or protein of the present invention (cDNA, transcript and genomic sequence). Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the enzyme peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.

As used herein, an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. However, there can be some flanking nucleotide sequences, for example up to about 5 KB, 4 KB, 3 KB, 2 KB, or 1 KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence. The important point is that the nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.

Moreover, an “isolated” nucleic acid molecule, such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized. However, the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.

For example, recombinant DNA molecules contained in a vector are considered isolated. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention. Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.

Accordingly, the present invention provides nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.

The present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.

The present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule. In such a fashion, the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences. Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.

In FIGS. 1 and 3, both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.

The isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.

As mentioned above, the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the enzyme peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA. In addition, the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.

Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof. The nucleic acid, especially DNA, can be double-stranded or single-stranded. Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).

The invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the enzyme proteins of the present invention that are described above. Such nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis. Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.

The present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3. Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents. A promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.

A fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.

A probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.

Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene. The gene encoding the novel enzyme of the present invention is located on a genome component that has been mapped to human chromosome X (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.

As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other. The conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. One example of stringent hybridization conditions are hybridization in 6×sodium chloride/sodium citrate (SSC) at about 45C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 50-65C. Examples of moderate to low stringency hybridization conditions are well known in the art.

Nucleic Acid Molecule Uses

The nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays. The nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2.

The probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.

The nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.

The nucleic acid molecules are also useful for constructing recombinant vectors. Such vectors include expression vectors that express a portion of, or all of, the peptide sequences. Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product. For example, an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.

The nucleic acid molecules are also useful for expressing antigenic portions of the proteins.

The nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods. The gene encoding the novel enzyme of the present invention is located on a genome component that has been mapped to human chromosome X (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.

The nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.

The nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.

The nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.

The nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.

The nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.

The nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms. The nucleic acid whose level is determined can be DNA or RNA. Accordingly, probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in enzyme protein expression relative to normal results.

In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detecting DNA includes Southern hybridizations and in situ hybridization.

Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a enzyme protein, such as by measuring a level of a enzyme-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a enzyme gene has been mutated. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain.

Nucleic acid expression assays are useful for drug screening to identify compounds that modulate enzyme nucleic acid expression.

The invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the enzyme gene, particularly biological and pathological processes that are mediated by the enzyme in cells and tissues that express it. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain. The method typically includes assaying the ability of the compound to modulate the expression of the enzyme nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired enzyme nucleic acid expression. The assays can be performed in cell-based and cell-free systems. Cell-based assays include cells naturally expressing the enzyme nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.

The assay for enzyme nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the enzyme protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.

Thus, modulators of enzyme gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined. The level of expression of enzyme mRNA in the presence of the candidate compound is compared to the level of expression of enzyme mRNA in the absence of the candidate compound. The candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression. When expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression. When nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.

The invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate enzyme nucleic acid expression in cells and tissues that express the enzyme. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.

Alternatively, a modulator for enzyme nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the enzyme nucleic acid expression in the cells and tissues that express the protein. Experimental data as provided in FIG. 1 indicates expression in humans in the fetal liver/spleen, breast, hypothalamus, ovarian tumors, lung fibroblasts, and brain.

The nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the enzyme gene in clinical trials or in a treatment regimen. Thus, the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance. The gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.

The nucleic acid molecules are also useful in diagnostic assays for qualitative changes in enzyme nucleic acid expression, and particularly in qualitative changes that lead to pathology. The nucleic acid molecules can be used to detect mutations in enzyme genes and gene expression products such as mRNA. The nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the enzyme gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the enzyme gene associated with a dys function provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a enzyme protein.

Individuals carrying mutations in the enzyme gene can be detected at the nucleic acid level by a variety of techniques. The gene encoding the novel enzyme of the present invention is located on a genome component that has been mapped to human chromosome X (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data. Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis. RNA or cDNA can be used in the same way. In some uses, detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos. 4,683,195 and 4,683,202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e.g., Landegran et al., Science 241:1077-1080 (1988); and Nakazawa et al., PNAS 91:360-364 (1994)), the latter of which can be particularly useful for detecting point mutations in the gene (see Abravaya et al., Nucleic Acids Res. 23:675-682 (1995)). This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences.

Alternatively, mutations in a enzyme gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.

Further, sequence-specific ribozymes (U.S. Pat. No. 5,498,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.

Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method. Furthermore, sequence differences between a mutant enzyme gene and a wild-type gene can be determined by direct DNA sequencing. A variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995) Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. Biotechnol. 38:147-159 (1993)).

Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al., Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl. 9:73-79 (1992)), and movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (Myers et al., Nature 313:495 (1985)). Examples of other techniques for detecting point mutations include selective oligonucleotide hybridization, selective amplification, and selective primer extension.

The nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality. Thus, the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship). Accordingly, the nucleic acid molecules described herein can be used to assess the mutation content of the enzyme gene in an individual in order to select an appropriate compound or dosage regimen for treatment.

Thus nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.

The nucleic acid molecules are thus useful as antisense constructs to control enzyme gene expression in cells, tissues, and organisms. A DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of enzyme protein. An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into enzyme protein.

Alternatively, a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of enzyme nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired enzyme nucleic acid expression. This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the enzyme protein, such as substrate binding.

The nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in enzyme gene expression. Thus, recombinant cells, which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired enzyme protein to treat the individual.

The invention also encompasses kits for detecting the presence of a enzyme nucleic acid in a biological sample. Experimental data as provided in FIG. 1 indicates that the enzymes of the present invention are expressed in humans in fetal liver/spleen, breast, hypothalamus, ovarian tumors, and lung fibroblasts, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in the human brain. For example, the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting enzyme nucleic acid in a biological sample; means for determining the amount of enzyme nucleic acid in the sample; and means for comparing the amount of enzyme nucleic acid in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect enzyme protein mRNA or DNA.

Nucleic Acid Arrays The present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).

As used herein “Arrays” or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support. In one embodiment, the microarray is prepared and used according to the methods described in U.S. Pat. 5,837,832, Chee et al., PCT application WO95/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93: 10614-10619), all of which are incorporated herein in their entirety by reference. In other embodiments, such arrays are produced by the methods described by Brown et al., U.S. Pat. No. 5,807,522.

The microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support. The oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length. The microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence. Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.

In order to produce oligonucleotides to a known sequence for a microarray or detection kit, the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit. The “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence. The second oligonucleotide in the pair (mismatched by one) serves as a control. The number of oligonucleotide pairs may range from two to one million. The oligomers are synthesized at designated areas on a substrate using a light-directed chemical process. The substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.

In another aspect, an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application WO95/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference. In another aspect, a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures. An array, such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.

In order to conduct sample analysis using a microarray or detection kit, the RNA or DNA from a biological sample is made into hybridization probes. The mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA). The aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence. The scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit. The biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations. A detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.

Using such arrays, the present invention provides methods to identify the expression of the enzyme proteins/peptides of the present invention. In detail, such methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample. Such assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the enzyme gene of the present invention.

Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T, An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).

The test samples of the present invention include cells, protein or membrane extracts of cells. The test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.

In another embodiment of the present invention, kits are provided which contain the necessary reagents to carry out the assays of the present invention.

Specifically, the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.

In detail, a compartmentalized kit includes any kit in which reagents are contained in separate containers. Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica. Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another. Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe. One skilled in the art will readily recognize that the previously unidentified enzyme gene of the present invention can be routinely identified using the sequence information disclosed herein can be readily incorporated into one of the established kit formats which are well known in the art, particularly expression arrays.

Vectors/host Cells

The invention also provides vectors containing the nucleic acid molecules described herein. The term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules. When the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid. With this aspect of the invention, the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.

A vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules. Alternatively, the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.

The invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules. The vectors can function in prokaryotic or eukaryotic cells or in both (shuttle vectors).

Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell. The nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription. Thus, the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector. Alternatively, a trans-acting factor may be supplied by the host cell. Finally, a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.

The regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage λ, the lac, TRP, and TAC promoters from E. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.

In addition to control regions that promote transcription, expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers. Examples include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.

In addition to containing sites for transcription initiation and control, expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation. Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals. The person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

A variety of expression vectors can be used to express a nucleic acid molecule. Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses. Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g. cosmids and phagemids. Appropriate cloning and expression vectors for prokaryotic and eukaryotic hosts are described in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

The regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand. A variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.

The nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology. Generally, the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.

The vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques. Bacterial cells include, but are not limited to, E. coli, Streptomyces, and Salmonella typhimurium. Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.

As described herein, it may be desirable to express the peptide as a fusion protein. Accordingly, the invention provides fusion vectors that allow for the production of the peptides. Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification. A proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety. Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enteroenzyme. Typical fusion expression vectors include pGEX (Smith et al., Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).

Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein. (Gottesman, S., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 119-128). Alternatively, the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al., Nucleic Acids Res. 20:2111-2118 (1992)).

The nucleic acid molecules can also be expressed by expression vectors that are operative in yeast. Examples of vectors for expression in yeast e.g., S. cerevisiae include pYepSec1 (Baldari, et al., EMBO J. 6:229-234 (1987)), pMFa (Kurjan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).

The nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., Sf9 cells) include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 170:31-39 (1989)).

In certain embodiments of the invention, the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors. Examples of mammalian expression vectors include pCDM8 (Seed, B. Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J. 6:187-195 (1987)).

The expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules. The person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.

The invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA. Thus, an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).

The invention also relates to recombinant host cells containing the vectors described herein. Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.

The recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).

Host cells can contain more than one vector. Thus, different nucleotide sequences can be introduced on different vectors of the same cell. Similarly, the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors. When more than one vector is introduced into a cell, the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.

In the case of bacteriophage and viral vectors, these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction. Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.

Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs. The marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.

While the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.

Where secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as enzymes, appropriate secretion signals are incorporated into the vector. The signal sequence can be endogenous to the peptides or heterologous to these peptides.

Where the peptide is not secreted into the medium, which is typically the case with enzymes, the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like. The peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatite chromatography, lectin chromatography, or high performance liquid chromatography.

It is also understood that depending upon the host cell in recombinant production of the peptides described herein, the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria. In addition, the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.

Uses of Vectors and Host Cells

The recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a enzyme protein or peptide that can be further purified to produce desired amounts of enzyme protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.

Host cells are also useful for conducting cell-based assays involving the enzyme protein or enzyme protein fragments, such as those described above as well as other formats known in the art. Thus, a recombinant host cell expressing a native enzyme protein is useful for assaying compounds that stimulate or inhibit enzyme protein function.

Host cells are also useful for identifying enzyme protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant enzyme protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native enzyme protein.

Genetically engineered host cells can be further used to produce non-human transgenic animals. A transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a enzyme protein and identifying and evaluating modulators of enzyme protein activity. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.

A transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. Any of the enzyme protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.

Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the enzyme protein to particular cells.

Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al, U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes. A transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.

In another embodiment, transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P1. For a description of the cre/loxP recombinase system, see, e.g., Lakso et al. PNAS 89:6232-6236 (1992). Another example of a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991). If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein is required. Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.

Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e.g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter G₀ phase. The quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal. The offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.

Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, enzyme protein activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo enzyme protein function, including substrate interaction, the effect of specific mutant enzyme proteins on enzyme protein function and substrate interaction, and the effect of chimeric enzyme proteins. It is also possible to assess the effect of null mutations, that is, mutations that substantially or completely eliminate one or more enzyme protein functions.

All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.

5 1 3812 DNA Human 1 cgctctagtg agcgcggacg gatgcttagg cagtagtcct ggcagcggca gtagtggtgg 60 cagcagaaga gaggaagggg gagggccccg agggctacac acgctcacac tttcaagttc 120 ccttggaggg agaggaggtg gggctgcaga aagaggaggc caggagcggt cccatccgtc 180 ccgtcccgtc ccgtctcccc ctcttcctct tgctccttgc cccccggctc tgcgagagtt 240 gagggttcag gtggccgtac gcggcagtga gggcaagagg gccgggagag tggggagcgg 300 aggcaggagt gcgggggaag atgcccatcc tgctgttcct catagacacg tccgcctcta 360 tgaaccagcg cactgacctg ggcacctctt atttggacat tgccaaaggc gctgtggagt 420 tattcttgaa gctgcgcgcc cgggacccgg ccagccgtgg agacaggtac atgctggtca 480 cctacgacga acccccgtac tgcatcaagg ctggttggaa ggaaaatcat gcaacattca 540 tgagcgaact aaaaaatctt caggcttctg gactgactac tctcggtcag gctctaagat 600 cctcatttga tttgttaaat ctcaatagat taatatctgg aatagacaat tatggacagg 660 ggagaaatcc atttttttta gaaccatcta ttttaattac catcacagat ggaaacaagt 720 taacaagtac tgctggtgtt caagaagagc tccatcttcc tttgaattcc cctctgcctg 780 gaagtgaact aaccaaagaa ccttttcgtt gggatcaaag gttatttgcc ctggtgttgc 840 gtttgcctgg agtggcttct accgaaccag agcaactagg gagcgtacca actgatgaat 900 ctgccatcac acagatgtgt gaagtcacag gaggtcgctc ctactgtgtg agaacacaaa 960 gaatgttgaa tcaatgttta gaatctctag ttcaaaaagt tcagagtggt gtagttatta 1020 attttgaaaa aacaggacca gatccacttc ctattggaga agatggactt atggattcat 1080 ccaggccaag caattcattt gctgctcagc catggcatag ttgtcataaa ctcatttatg 1140 tacgacctaa ctctaaaact ggtgttcctg ttggacattg gccaattcca gaatcttttt 1200 ggccagatca gaatttacct tcactacctc cacgaacatc tcatcctgtt gtgaggttct 1260 cctgtgtaga ttgtgagcca atggtaatag acaaacttcc ttttgacaaa tatgaacttg 1320 aaccttcgcc cttaactcag tatatcttgg aacgaaagtc tccccatacc tgctggcagg 1380 tatttgttac tagcagtgga aagtacaatg aacttggata tccatttggt tatttaaaag 1440 ccagtacaac tttaacttgt gtaaacctct ttgtgatgcc ttacaactac ccagttttac 1500 ttcctctttt agatgacttg tttaaagttc acaagcttaa gccaaatctg aagtggcgac 1560 aggcttttga cagctactta aaaactctgc ctccatacta cctattaacc aaactagagt 1620 cagaacgaat actagcatca gtggggaaga aacctcccca ggaaattgga attaaagtga 1680 aaaatcattc tggaggtggc atgtccttga ctcacaataa aaattttaga aaactattga 1740 aagaaatcac aggggaaact gcacttagac tgacagaatt gaacaccaaa gaatttgctg 1800 gcttccaaat tgggctctta aacaaggatt tgaaacctca gacatacaga aatgcttatg 1860 atattccccg tagaggtctt ttagaccagc tgaccagaat gagatccaat ctgctgaaaa 1920 cgcacaagtt tattgttgga caagatgaag attcccttca tagtgttcca gttgcacaaa 1980 tgggtaacta tcaggaatat ctgaagacat tggcttctcc actgcgagag attgatccag 2040 accaacccaa aagactgcat acttttggca atccgtttaa acaagataag aagggaatga 2100 tgattgatga agcagatgag tttgtagcag ggccacaaaa caaagtgaaa cgtccagggg 2160 aacccaacag tcctatgtca tctaagagaa ggcggagtat gtccctgctg ttgaggaaac 2220 cacaaacacc acctactgta actaaccatg tgggcggaaa gggaccaccc tcagcctcgt 2280 ggttcccatc ttatccaaac ctcataaaac ccacccttgt acatacagat gctactatca 2340 ttcacgatgg ccatgaggag aagatggaaa atggtcagat cacacctgat ggcttcctgt 2400 caaaatctgc tccatcagag cttataaata tgacaggaga tcttatgcca cccaaccaag 2460 tggattctct gtctgacgac ttcacaagtc tcagcaaaga tgggctgatt caaaaacctg 2520 gtagtaacgc atttgtagga ggagccaaaa actgcagtct ctccgtagat gaccaaaaag 2580 acccagtagc atctactttg ggagctatgc caaatacatt acaaatcact cctgctatgg 2640 cacaaggaat caatgctgat ataaaacatc aattaatgaa ggaagttcga aagtttggtc 2700 gaaaatatga aagaattttc attttgcttg aagaagtgca aggacctctg gagatgaaga 2760 aacagtttgt tgaatttacc atcaaggaag ccgcaagggt taaaagacga gtcctaattc 2820 agtaccttga gaaggtacta gaaaaaataa attcccacca ccttcacaac aacattagtc 2880 acatcaacag cagatcatca tgttagtgca aagaccagtg agaaaaaaat gacaagtttt 2940 ctgtgctgta ggatggaaca ggatattgtt gaagcctcct ggaatgtttg agtcaaggga 3000 attgctttcc agatgctaag aagcagcagt ggggcttttg aattttatga ttatctggca 3060 gtgaaagctg ggcttttgcc ttaataattt tttaaagtat gaattgtttt gttttgtttt 3120 cctcaattga ggaagctgat gttattaatt cacaggctaa attcggtaaa caccactgcc 3180 cctaccacgg gtaatgagag gtcactcact tgaactttgc cattccaggc attctcagag 3240 tggcgagggg ccacctgcaa gtggagcaca acttggtgct cttactgtgt ccttcagaaa 3300 gaataggtgt acagaaagga aatggcaatc ttatgtgtgc tgaacaaagt tttcaacaat 3360 tcctagttgt gccttttaaa ccatgcaata ttcaggatag tttgaatcaa agaagtaaga 3420 agctgctatt tgggtaactt atttctctgt gggaaggggc agggagagtc accaaacaat 3480 ctacctccaa ctctcttctc ttttgtctag agacattaca aagtgcactt gaggctgccc 3540 ccaacctctg acatttgttc ttgcatgtga tgatagaaag tcttcagatg gacttataca 3600 ttctgtgctt tggaagcaca agaagaacaa aatatgtgta tatttccttt aatgtttata 3660 caaaagttta tatggagcag tattgttatg tttgtatgaa tttgcaaaaa ttaaagtgta 3720 caaagagatt ttgattttgc atatataaaa taaatcattt tattgatttt caaaaaaaaa 3780 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 3812 2 861 PRT Human 2 Met Pro Ile Leu Leu Phe Leu Ile Asp Thr Ser Ala Ser Met Asn Gln 1 5 10 15 Arg Thr Asp Leu Gly Thr Ser Tyr Leu Asp Ile Ala Lys Gly Ala Val 20 25 30 Glu Leu Phe Leu Lys Leu Arg Ala Arg Asp Pro Ala Ser Arg Gly Asp 35 40 45 Arg Tyr Met Leu Val Thr Tyr Asp Glu Pro Pro Tyr Cys Ile Lys Ala 50 55 60 Gly Trp Lys Glu Asn His Ala Thr Phe Met Ser Glu Leu Lys Asn Leu 65 70 75 80 Gln Ala Ser Gly Leu Thr Thr Leu Gly Gln Ala Leu Arg Ser Ser Phe 85 90 95 Asp Leu Leu Asn Leu Asn Arg Leu Ile Ser Gly Ile Asp Asn Tyr Gly 100 105 110 Gln Gly Arg Asn Pro Phe Phe Leu Glu Pro Ser Ile Leu Ile Thr Ile 115 120 125 Thr Asp Gly Asn Lys Leu Thr Ser Thr Ala Gly Val Gln Glu Glu Leu 130 135 140 His Leu Pro Leu Asn Ser Pro Leu Pro Gly Ser Glu Leu Thr Lys Glu 145 150 155 160 Pro Phe Arg Trp Asp Gln Arg Leu Phe Ala Leu Val Leu Arg Leu Pro 165 170 175 Gly Val Ala Ser Thr Glu Pro Glu Gln Leu Gly Ser Val Pro Thr Asp 180 185 190 Glu Ser Ala Ile Thr Gln Met Cys Glu Val Thr Gly Gly Arg Ser Tyr 195 200 205 Cys Val Arg Thr Gln Arg Met Leu Asn Gln Cys Leu Glu Ser Leu Val 210 215 220 Gln Lys Val Gln Ser Gly Val Val Ile Asn Phe Glu Lys Thr Gly Pro 225 230 235 240 Asp Pro Leu Pro Ile Gly Glu Asp Gly Leu Met Asp Ser Ser Arg Pro 245 250 255 Ser Asn Ser Phe Ala Ala Gln Pro Trp His Ser Cys His Lys Leu Ile 260 265 270 Tyr Val Arg Pro Asn Ser Lys Thr Gly Val Pro Val Gly His Trp Pro 275 280 285 Ile Pro Glu Ser Phe Trp Pro Asp Gln Asn Leu Pro Ser Leu Pro Pro 290 295 300 Arg Thr Ser His Pro Val Val Arg Phe Ser Cys Val Asp Cys Glu Pro 305 310 315 320 Met Val Ile Asp Lys Leu Pro Phe Asp Lys Tyr Glu Leu Glu Pro Ser 325 330 335 Pro Leu Thr Gln Tyr Ile Leu Glu Arg Lys Ser Pro His Thr Cys Trp 340 345 350 Gln Val Phe Val Thr Ser Ser Gly Lys Tyr Asn Glu Leu Gly Tyr Pro 355 360 365 Phe Gly Tyr Leu Lys Ala Ser Thr Thr Leu Thr Cys Val Asn Leu Phe 370 375 380 Val Met Pro Tyr Asn Tyr Pro Val Leu Leu Pro Leu Leu Asp Asp Leu 385 390 395 400 Phe Lys Val His Lys Leu Lys Pro Asn Leu Lys Trp Arg Gln Ala Phe 405 410 415 Asp Ser Tyr Leu Lys Thr Leu Pro Pro Tyr Tyr Leu Leu Thr Lys Leu 420 425 430 Glu Ser Glu Arg Ile Leu Ala Ser Val Gly Lys Lys Pro Pro Gln Glu 435 440 445 Ile Gly Ile Lys Val Lys Asn His Ser Gly Gly Gly Met Ser Leu Thr 450 455 460 His Asn Lys Asn Phe Arg Lys Leu Leu Lys Glu Ile Thr Gly Glu Thr 465 470 475 480 Ala Leu Arg Leu Thr Glu Leu Asn Thr Lys Glu Phe Ala Gly Phe Gln 485 490 495 Ile Gly Leu Leu Asn Lys Asp Leu Lys Pro Gln Thr Tyr Arg Asn Ala 500 505 510 Tyr Asp Ile Pro Arg Arg Gly Leu Leu Asp Gln Leu Thr Arg Met Arg 515 520 525 Ser Asn Leu Leu Lys Thr His Lys Phe Ile Val Gly Gln Asp Glu Asp 530 535 540 Ser Leu His Ser Val Pro Val Ala Gln Met Gly Asn Tyr Gln Glu Tyr 545 550 555 560 Leu Lys Thr Leu Ala Ser Pro Leu Arg Glu Ile Asp Pro Asp Gln Pro 565 570 575 Lys Arg Leu His Thr Phe Gly Asn Pro Phe Lys Gln Asp Lys Lys Gly 580 585 590 Met Met Ile Asp Glu Ala Asp Glu Phe Val Ala Gly Pro Gln Asn Lys 595 600 605 Val Lys Arg Pro Gly Glu Pro Asn Ser Pro Met Ser Ser Lys Arg Arg 610 615 620 Arg Ser Met Ser Leu Leu Leu Arg Lys Pro Gln Thr Pro Pro Thr Val 625 630 635 640 Thr Asn His Val Gly Gly Lys Gly Pro Pro Ser Ala Ser Trp Phe Pro 645 650 655 Ser Tyr Pro Asn Leu Ile Lys Pro Thr Leu Val His Thr Asp Ala Thr 660 665 670 Ile Ile His Asp Gly His Glu Glu Lys Met Glu Asn Gly Gln Ile Thr 675 680 685 Pro Asp Gly Phe Leu Ser Lys Ser Ala Pro Ser Glu Leu Ile Asn Met 690 695 700 Thr Gly Asp Leu Met Pro Pro Asn Gln Val Asp Ser Leu Ser Asp Asp 705 710 715 720 Phe Thr Ser Leu Ser Lys Asp Gly Leu Ile Gln Lys Pro Gly Ser Asn 725 730 735 Ala Phe Val Gly Gly Ala Lys Asn Cys Ser Leu Ser Val Asp Asp Gln 740 745 750 Lys Asp Pro Val Ala Ser Thr Leu Gly Ala Met Pro Asn Thr Leu Gln 755 760 765 Ile Thr Pro Ala Met Ala Gln Gly Ile Asn Ala Asp Ile Lys His Gln 770 775 780 Leu Met Lys Glu Val Arg Lys Phe Gly Arg Lys Tyr Glu Arg Ile Phe 785 790 795 800 Ile Leu Leu Glu Glu Val Gln Gly Pro Leu Glu Met Lys Lys Gln Phe 805 810 815 Val Glu Phe Thr Ile Lys Glu Ala Ala Arg Val Lys Arg Arg Val Leu 820 825 830 Ile Gln Tyr Leu Glu Lys Val Leu Glu Lys Ile Asn Ser His His Leu 835 840 845 His Asn Asn Ile Ser His Ile Asn Ser Arg Ser Ser Cys 850 855 860 3 65042 DNA Human misc_feature (1)...(65042) n = A,T,C or G 3 ccctagccca tgtaggcatt gcccttctac actgacattt gtatcggaat ggaaatgggg 60 gcttctagta tctttttcat ccttatttct tcattaattc cctactttcc accagaatgg 120 cctgaaatgc accatacata gtactatctt tggctgagtt tttgttcata tcattccttc 180 caacccagat tccctctctt ccctttttgt gccttgttcg tgaaatccta tgaatttcta 240 gactggacca ttgtttccat agcacttttt aacttgcatc cttgtttgtc cctgattcat 300 atactgccat atgacttctt ttaaaatcgt atttctctga gaatgttatt gaatgtgcat 360 atataatata tgaaacatat acacagaaca tacatatata tatatatata gagagagaga 420 gagagagaga gtgtatataa aatatataaa atactttttt gagatgttat ctcattctgt 480 tgcccaggct ggagtgcagt ggtgtgatct cagttcactg caacctccgt ctcctgggtt 540 gaagtgattc tcctgcctca gcctcccaag tagctgggac tacaggcgcc tgctcccatg 600 cccggctaat ttttgtattt ttagtagaga cgggggtttc accatgttgg ccaggctggt 660 ctcaaactcc tgccctcaaa tgatccaccc aactcggcct cccaaagtgc tggaattaca 720 ggcatgagcc actgcgcctg gccaaaatat ataaaatatt atgtatgtat atgtcatcat 780 ctctcctcaa tgaaactgca aactcattga agtcctggat tccacattgt caatagtaat 840 tgccaggaat acacaagtcc aatttttaaa attgtgtcat atgaagtagt caatcaagtg 900 tggttggcca cttactgagt ctcttcacag agccagacct gagagtatcc gtaattgtta 960 ccctaacctc agggagctgc attttcctct actgaaaatt gaatacaatg ccatctgcca 1020 taattaattc aaagattaaa caaggctacc gtgggtgcct ggctcttcat aggcactcaa 1080 taaatgtgag ttgagagcct gcccctgtgg tcccagctac ttgagaggct gagatgggag 1140 gatcgcttaa gcccaggagc tggacgctgc aggcagctat gatggggcca ctgcactcca 1200 gcctgggcga tcaagcgaga tcctctttat ttatttataa aaataaataa ataaataaat 1260 atgtgagttg aatcacaatc taggtttgca aacctccatg tgtaaaggct gcgcagaggg 1320 aacagtggtg gaattatcac aggcaggcca atgtttcaaa gagcttagtg aaactgaaga 1380 agcttgtgca tacaaaaggc cagtttaggt aactgtaact gtgtttaagc tttagtttcc 1440 tttctaagta gatatatgtg gaatgcaagg ccagcaacca actcacaaat actgatcaag 1500 acgggggagg gatctaaagg aatgtgagta cgtcctgcca ggaaagaagt ttgctgcttc 1560 tgaaatattt tcgtcttcgc cactggcagg attgatcgat tgcagttagc gaagaatttt 1620 ctgtgcaaac tgtccaagca tctgcttctg tacttctgta caactgttgc tcaaattcac 1680 tcttcttttc gaatcaccat ctttgaagag agacagaaaa atccatttaa accacccgaa 1740 ctaatcattc gaactgcttc caagtccttt aaaggagaat cctagcgagg gtccgtaaca 1800 cttcccctta ccctctgcct gggttcaaac ttcaactccc agggttcgcc caagtccctc 1860 ccctagtcct gtcatctaat gaatatgcaa ataccacata attggcagcc aatggcatgg 1920 gttctggtca catggtgccg atggtaggtg agcagacaga agttgtcagt gaacagagac 1980 ggcgctcagt ctggggcgag cgctctagtg agcgcggacg gatgcttagg cagtagtcct 2040 ggcagcggca gtagtggtgg cagcagaaga gaggaagggg gagggccccg agggctacac 2100 acgctcacac tttcaagttc ccttggaggg agaggaggtg gggctgcaga aagaggaggc 2160 caggagcggt cccatccgtc ccgtcccgtc ccgtctcccc ctcttcctct tgctccttgc 2220 cccccggctc tgcgagagtt gagggttcag gtggccgtac gcggcagtga gggcaagagg 2280 gccgggagag tggggagcgg aggcaggagt gcgggggaag atgcccatcc tgctgttcct 2340 catagacacg tccgcctcta tgaaccagcg cactgacctg ggcacctctt atttggacat 2400 tgccaaaggc gctgtggagt tattcttgaa ggtaaaggga ggggagggga gagatgggga 2460 gagctcccga gggatttcag ggtgtggatt gaggtgcttc tgtaacgttt gtatcgccct 2520 cccccctcct ttcctacgcg accccctccg tcatcccttg ccccgcagct gcgcgcccgg 2580 gacccggcca gccgtggaga caggtacatg ctggtcacct acgacgaacc cccgtactgc 2640 atcaaggtaa aggggctacg ggtgggggga caggcgggaa gcgggagcaa gtcggcgggg 2700 gctgcttacc cccctgcccc cgcctaaggc ggtcctgcgt cgcccggcgg ggcgggcggc 2760 gagggggtgc gcagagggcg ggcggagtgg tgccgtcggc ggcttcggag tagctgtcgc 2820 gcctggggtc ggggagaggg gaccggggag gagcagcccc ggggagaaac cgcaggaggg 2880 ccgagctcgt ggcgcgacaa ccgcagccgc ctcggaacat ggcggacatt ttgcttttgt 2940 atgagcctgc gagagggaga ctgagggcgc tgctgagatg gaaaggaggg aggggaggga 3000 ggagcgggta aggagggccc gaaacccgga gggaggctgc gaggcgggcc cgccccttcg 3060 aggcgcaccg cgcgagggtg cggccgcggc cggggggccg gacggagcct gcgactccgc 3120 cccgaggtcc tgccggccgg gcgcgcgggc tttcccggag cctgggctcc tcctctggcc 3180 cctccttcct cccccggtct tcctccccct ccttgggctc ttcgctgcat ctcctccttc 3240 tccccctctt cctcctggtc ccctcccctt cctgctgaga gcgtggcaga gccagccgcc 3300 ggccttcaaa gactagacaa ccgcctttgc actcgttggc ctctcaccac ccccgcgcaa 3360 tcggaaatct gtccacgacg ccagtctccc cacccccaga cccggagaaa gtctttgcgt 3420 ttctgctccg gaattggcca ggttcagccc cgctctcagt taccttagct actgttactg 3480 tttcattgga aattccagcg aagcaacgac acggaggggg acgtgccaag tgcgaaccca 3540 caggggcaga gctttttagg gatccgctct acctatttac atcataaatt aggtttgtgc 3600 tagccacgta ggaattaatc cagggacaag aaagaaagga aggggaggac tcaaatgtga 3660 gcatttgtaa tagtcaagtt cgatgatttg attctgacct acaggagaaa agtagggagg 3720 acggtctctg tgggggaatt tatgttccta tggtgaggag ataaagaact gctgctttgc 3780 ctgcagtggc cagataaaat ggaatttaaa ctgttaaatc aacctgcata agagtcctgc 3840 ttgcatattg aaattttaaa aatactacca caatccttga cgtcttttgt taggcttttt 3900 cttttttcct cagaataatc gtaatagtgc tagggagacg cagtctggat gtgttgtgat 3960 ccgtttctgt agagtgaggt gttttaatga atggaaccta ccaagctgaa tagttggcca 4020 aagagtgttc cttcaagcat aaggaaacca aagagaaact aattttgtaa ctcgtagctt 4080 cggttaactg tttaattagt aggttcccct taaaactgtt cttttttcga taatttgttt 4140 tcagtttgtg attctatcca tttagaaaag tggaacaagt agacatcttt caaaatgccg 4200 taagcttttt aaaaatgtca gttttcccaa aaggatgtga tcattttttt ccacatagaa 4260 aaggagatgt ttatacatcc taggtctgaa tgtctacact cttcgactgc taatacagat 4320 aagaaccgac catttgtagt gtggccattt gaagacatgc tccttaattc gaagtagtaa 4380 aaaagataaa ccacaaagca gtgtgccttc ttttccttaa aggaacaact tattggccgg 4440 gtgcggtggc tcaggcctgt aatcctagca ctttgggagg tcgagatggg cggattgcct 4500 gagctcagga gtttgagacc agcctgggca acatggtgaa accccgtctt tactaaaata 4560 caaaaaaaca aaacaaaaaa aaaaacggcc ggatgtggtg gcgggcgcct gtaatcccag 4620 ctacgcggga gnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4680 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4740 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4800 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4860 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4920 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 4980 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5040 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5100 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5160 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5220 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5280 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5340 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5400 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5460 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5520 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5580 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5640 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 5700 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nncttactat atagctgtgt gctcttttaa 5760 aattagtcat accttttact tgcagtcccg gtttgcatgg atagaattaa gtttgactta 5820 agtaccacat aaaaagcgta cgaaatgtaa gcatcatgtg ctacatctgt tatgttgctt 5880 tctagacaag ttttatgcat agtgttacaa gtgttgaccc cacctttata ccgtggtatc 5940 ttcagtgtac acagctagta tgaaaccctg tttaacattt aaaaacgtct aatgtatcct 6000 tataaaacta gtatgtggtt tttaaaagtg ttaatgtttt gggatttttt ggtataattg 6060 ttgtttttag tcttggctga ggttctgctg tcttgtatgt tttgttttgc tatgaatcat 6120 aatttccttt tatttagtga atagaagagg caggcttgtc actactatta ctttgaaaga 6180 aagtaagcca ttagagtagg gtatatatta acaaaggtat tcaaaatagt tttatgttgg 6240 aagctactta aaattatttc ttttttgttg aaggaaatta tctttttaaa cataaaatgg 6300 agttactttt ctagaaatag ttgaaacaca tgtataaaat actggccaga agatttttat 6360 aaataggaaa tgataatgtt tcaaagaaat atcctaagtc tgtaatttga agacatacat 6420 ttgaaaaagt aaaattttcc ctgagtgttg ccttttccca tcctgtagct agctttgctt 6480 actggtgtct gcatgccttt gacaacatgt atcagaaaat agcaaaattt tggcttacag 6540 atttaggaag taatttaagc ttttaaaatg atatgtgtta caggcatttt ttagaatttt 6600 aactaagaca taactttttc atatgcccat gaatatattt tatagatctt atttgcaaaa 6660 ggagtgactt ttatgggagc ctttcattgt ggttaagaag ctatggaaga gcttatcagt 6720 gaaatagtag caacatggcc tgtgagagca atcttagaca atgaaagatg cttttaaaac 6780 tcaaaaagcc acacaggcag tgcattgact tttacaacga attgcctctc ccatgatctt 6840 gctttcttat ccaccttcct ttactggcca tttgtggcat gcagcaataa ttattttgaa 6900 ataagaaaag gagagagtca acagtagaag actagacctc tgggcaatac aatcttcaga 6960 ctaaggacca gctgtaagat gactagggaa gatgcctgac aaaactgtgg aggtctgtct 7020 gttctgtatc cccaacctct ctcgtatcca ttcattctta tttgctcctc gtttcaacct 7080 tcatcatttc tcacttgcaa gcagccactc agttgttctc cctacttcca gtcttgctct 7140 ccactgattc cttcccgtca ttgccctcag attgatcatt ctttaaataa aataaagtca 7200 ttcccctatg aaaaaaaaat ccttcagtgg cactccatta catttcccaa taaaagtaaa 7260 tttcttggcc tggcctccat ggccgttcat gatctggccc tatcttacca tgtctctgcg 7320 ccctctcttc tcttctcatg gacctcaggc ttcacccaca atgaaaaatt aggtcctcct 7380 ctccaaacac actatgccag ttgcttctgt gccattgtaa atgttattcc ctctgcctgg 7440 gacacattgg ttggccagac atacctcagt tctttattct atgttttcaa aagtcatttt 7500 gtccgtcggc tttttcccta ctccaagcag tataacaact tcctctgtga tcctttaaca 7560 tgttgtccac accttaacta tatagcattt agcatgttat atggggacta ttagtgttca 7620 tgttgacttc cctaatgtga gctcttgaag ggcaaatatt tgaacttcta ggtatttgta 7680 tccctagtac ctaagggggt gtttagattt taatatgtac tcaacaaatg gaaaaaggtt 7740 tcaagcaata tgttaagtgt caaagctact catttccctc atgtcaaagc ttacctcatt 7800 cccggtactc ttccccatag agtaatcact attaacaatt tgatatattt aatgtttatt 7860 acagctagca ttttcatata ggttcaagtt tataatatgg tagaatctta ttgtattttt 7920 tacaagataa gtgtatatat ttctcttttt tcttttttat agaagtataa ttcatatata 7980 gaaaatacat gaatcctaat gacttgatgc atttttatat ttatacattc atgtaaccac 8040 catcccaggc caagatatat aacgtttcca tcaaccagga aaatgcctct tgcatctttc 8100 tgcaatccat ctctcccctg catgtaatta ccgttctgac ttttatcacc attgtagtga 8160 catgatcaaa atggtgtttc caaaagacaa gtgtaacagt gggttgacac tacggcagtc 8220 tcggcattca tttaccatat acttcttgaa catctcctct gcaccaggct ctgttatagg 8280 ggcctaaggt gaaaccagaa agatctggcc taagaaggga ccagaatagt aaaagacatg 8340 gtcctagtca ttaaaggtct tgaggatagt cactggaaaa agctgactag agaaggtggc 8400 ttaggatatg ggaaatgtaa agagcagtgg actcttaacc agagaattgg aggtgaggga 8460 ggaggatgca caggactctg agaatctggt gtgtctcaag actataacta gttaagactg 8520 gaccacagaa aggctttgaa acttgtaagc tagattttgt acatttcttc tgggatgcag 8580 agctcttagg tagaattgaa gagaaatagg acaaagcttg ttgtctatat gcttgtttgg 8640 ttataattac cttttaagtg agctaaaggg aggggagaat aaaaggctag ggagacccat 8700 aagttgtagt tgaaattgcc tagttttgtt gcttgctgct tgagagcttt tggccttatg 8760 gttgggattg gggtgggggt agggagatgg tgaagggcag ggcacaggta aggaaagggc 8820 agatattttt tcttttcagt ttgcctttgc tttgggaaga taattataat ttagaacaca 8880 gggttctcag tttcacagag tgaaaaaata tgatagtggt tccacatctc aggaagaaat 8940 gtgttttcta gagaagggta ggattgaagg accctcctta tgggagtgag aagggcagtg 9000 aagaaaggaa actacatgtt tcatttaagt tcttaaatga aaaagtcttt gtaaacatgg 9060 cctcctcccg gttgcctttt accgaaagag tgtaaatgag agacccaggc agtccctttg 9120 taactgtgta ttgggagctt ggaacacatt atctcctgga tacaatgttg gaagtggtga 9180 ttatgttccc agaccttccc tcccaggaac ctttttaacc cttcatgtca cttagccata 9240 gacctattgt gtttataatt gtttctaatg ggaaatgggt ttaagtttcc agcttgattt 9300 gttaaaaaca tattctttct ctcttcttcc tcacaactgg gtgtggactt tggttccatg 9360 aggggtgggg acactgtaaa ggctccggca gagagggtga ggggctgagg tggcagtgga 9420 ggtaggcgtg gctcttcaca tatgccagtt actcctattc atagattggc tacatttaca 9480 cggttcagca tagcgtccac ttagccacgt atggttattg agcacttgaa aggtggctag 9540 tctgtcagtg ggtgcttcaa cagacagtgt aaaatataat attttggata tattaagtaa 9600 attattaatc taacttgttt ctttttactt tttcaatgtg gtgagttgaa aatttgaaat 9660 tccatatgtg aaatttgcac tatatttcta ttagcagtgt ttgtctatat tctttcttaa 9720 gatattttat gatgttcata tcctaggaat tgtttctgaa ggaggatcct ttctctggaa 9780 gttccgttta aaatgaacac cccccccccc ccgacccacc gcaataaaag actcatttgt 9840 gcatgaaagg ttatcataca gttcagagtt gatggcttga taacccttgc ctgtggggca 9900 aaatatgaaa gcatcccatt cttatttgta ttgaaagcca gtttggttgc ttagtctttt 9960 ggatgcagtt ggtgatccaa ctggttgggt tagaagtctt ttcctgggct aagtataatg 10020 gaatatgtat gtgaatgaat gtaactgcag taattcagaa ttctgtttat aatatgtgct 10080 caccagtagt gctaaatgtt tcatactttc agtgttatta gaaatatgta acatgtccgt 10140 tgtttgattt acatagctac tttgcccaag aattctcagg agcagcattc tttaggaagt 10200 gtaggataaa ggagaaatac tctagtttgt catagtgtaa aacttaacaa aggggaattt 10260 gtatcactgc tgtttttgag agctttcttg atgttcccca gcggagccct tgtcttatat 10320 catggcaagt catcagtggc gttaaaagga gggagaggcc acatgactgg agggctccta 10380 ggattcttac ttctgacagt cgttaacttt ctcaaaactt aatcctccta gtggaggtta 10440 caggagtgat taattgttat tttttggtaa ctataatggc tcccatttaa ggaataagca 10500 ccaatgtcta attctgaggc tgggtggatt tatagatatg ctgatgaata gcatctataa 10560 gaggtaggac cactttatag ccctaatttt ggatcctcct aaatcccatc ttatagtcga 10620 aggtgttatc tagcttgtat aactatccct gtatttcaga tatgatttga cttatatttg 10680 cttccttgta ataatgaaca atcacgaaat agccttcaaa taatagcagc tgacatttat 10740 tgagtaatgc ttaggtacag ggcaatgtgc taatgaatgt aaaatgttta tttagtttct 10800 cttcctagtc agtctgtgta ctggattact aggtactatt attatactct ttttatagat 10860 aagggaacca gggcccagag aggttaagta acccagccag tagtaaccta ggtctgtctc 10920 tattctagtc tattcagtga ttaaccactt cacttctcct atcaattgtg acagaaaatt 10980 ccttttgata acttctcact ggtattttct cattatgatg catgtcctag agccatcatt 11040 ttttaaacat aattatcatg ctgttattta tagctgcttt taatgtaata gtgcttggca 11100 ttgtagcaag cactcaatga atgaaaatta ttactgctag tgttattatt tctaatattt 11160 ctctgactgt tgctgggtga gtattgtggt gcatatgttt gtaaaacact tttgcctttg 11220 atgtcccaca gttatgcccc tactggtgac agatatagag ttgttgagac tctcagttga 11280 tggagtatga aatagttgag gactggagga tgtgaactgg tggcctaggc tgaggaggcc 11340 ctataggaat agtggtaggt ttgtaaaagc agcagggtag tccttggcta tttattaata 11400 atagccacta aaaactgata tgccgtcttc actttaccaa tctcctgata aatgcttttc 11460 ttatgaggaa aagaaagata ttcagtgtac tccacagtag ccatttgttt tttctaatcc 11520 acagcctctg gaggaggtag acatggtttt taaaaacgtc tggaatacca tcatgccttt 11580 gcagagtttt gtgtatcagc ctgagcctta tctgctggtg tggtcttcat ttcaactact 11640 tctcccattt tcctcaagcc acacacctgt catagccaga tcattggttt tttcccctcc 11700 tgtgtagtta gatggcctgg ggtagaagag tggattttat agaagaagta gagatgtcag 11760 tcagtggggt cttaaccaga gaaacattgc atgaagactt ttgggtgatg tgccagatgt 11820 ttatagaaaa agtagaattc tatatcttaa accattttcc cctggttata ctactcatta 11880 atgccagtcg ctcttttatt atctatatcc tgccctgtag ctcaaatagt tcagtgaact 11940 tagtaccagg agccaaacac aggatttgaa tgcaattgaa caaaagtctt gaaacatttt 12000 tgtttgtgca actgaaaaat agtactgtta agaaaactaa atatgattta ttaaggtctt 12060 aagatttact gtcgagctac ttgggcaaag ttactaatat tcatcctctt tgtccttgac 12120 tacatttgaa actaactact tcttccttcc agaaacttat cacttcctat attctgtttc 12180 tccactcctc tctctgataa ttctttctct atcttccaaa gtctttccct tggggagtgt 12240 atcctgcttc attcgtggtt ccaaatattc cgacacacac tgatgcttca ccatcttcag 12300 cttctcactc aggcatctca gctgagtgca ggacatctcc acacatctcc actgactgtc 12360 tgtcctgctg tcagctcaca gtcagacctc ttctgtcatt attcagcttt gttttttctt 12420 tttgccttcc atcttctctg gcttatctgc catccctttg aaatttctct tacatgtgtt 12480 cctttgactc aatttctgtt gccatcactt taatctaggt cctcatgttt ttatgctttg 12540 accactgtac cagccttcta actggactcc caagtgcctc caaaattcct gtctccactt 12600 acatcaattg ctaactttcg aaaaaagttg gttttatcat atcaccctcc ccaccagcct 12660 gccattctga gctctctagt atctgttcca cgtgtcggta aaaacttatt tcccatcatt 12720 tcccacagaa gccctgcact gtctcttcta ccctctgagt gtatctcccc attcctgatg 12780 ccagccctta gaacatcagt taaccaaagg aagaagagat acagagccag gagagctgaa 12840 ggcctggggg aggagaggaa gtaaactgaa atcattccat taagggtgtg acttgagggt 12900 gaggacatga cagaacatgc tttaaaatac tattataatg atgagaagtt gcagaaggaa 12960 ggagggtggg agctggagta tgacctttcg tgtttgatta gtctgaactc tagaccaaaa 13020 tggtttcatt taaattggcc tgaagttgcc tggaggcact gctgtttaat cagaagggcc 13080 agtccctctt tgaatttttg tctctgccaa agacagccca cataactaga cagtggacaa 13140 taggattcca gggagaatat ctagccttta atatagccat ggcattggaa agtggagacc 13200 ccctcctgtt ttatttcttg aaggaggatg ttggcgatat gcagagcaaa gctctccact 13260 tttcttaata gcttacgtag gtgcgtaaac attgtaaact ccctttcata gtgatgcctt 13320 tgagttgtgt gttagaagta gatttaggct atagctaggt acttttataa aatcagattt 13380 taaaaagtgg acatagtaca tccagtctag tagatcatac catctactgt catgtaatat 13440 ggcaaactgt atcattgtca cttcagtagc tctgtcaaaa gtgctggact ggaaggcaag 13500 agatccatgt tcttaacctg agtctgttac taattacaca catgacccca ggcaagtcac 13560 ttaacctttt atggtgtcag tttcctcatc tgttaaatga agggattaga ctagattatt 13620 tccaggactc cttccgaaaa agtacaggag agagttgtat aactgaaagg cagaaagtgg 13680 aataattgag gcttggaatt cagggtgact taaaaattac tttaggctgg acatggtggc 13740 tcacacctgt aatcccagca ctttgggagg ctgaggtggg aggaccactt gagcccagga 13800 gtttgagaca gcctaggaaa cacggcaaga ccttgtctct acaaaaaata attaaaaaaa 13860 aattagcctg gcatagtggc acatgcctgc agtcccagct tctcaggagg ctgaggtggg 13920 aagatcactt gagcccagga ttacaagact gaagttagct atgttcacac cactgcagtc 13980 cagcctgtgc cacaaagtga gatcctgtct caaaaacaaa aacaaaaaca aaaacaaaaa 14040 aacaactttt aaattttaga aaacaggtcc tggatgtgtt taatgtgcta tatcacacac 14100 ttagtggtta cattggtaaa tgccactcca tcttattgat gtcaattctg tttgctgtaa 14160 acaatttaat aacgttcatg acagagtcct atcaatactt tggaagagtg agagtgaggg 14220 tttggtgaac agacagacta actttgtatt ttgttgggat ttttaacaat gaatgcatgt 14280 tacttttacc acgtaaaaag tagctcataa caattttttt gaaattattt attttcatta 14340 acttttattt taagttctag tgtacatgtg caaaatgtgc aggtttgtta acatgtgcca 14400 tggtggtttg ctgcatagat catcccatta cctatgtgtt aagcccagca tccattagct 14460 attcttcctg atgctctccc ttcccccacc cccattcaca ggccccaccc agtgtgtgtg 14520 gttcccccca tgtgcccatg tgttctcatg gaagaatttt tcctaaaaga attagtcctg 14580 gggaaagagg tgctgtgtaa tcttcagaac gtaataaatg gccattctgc tatctcatat 14640 gttcaacact ttctgcaatg cttaggtggc ttagtctcac tcctgtccat gtatgttttt 14700 tccaaggcca aaaattttta ttattttgtg tatctgtcca taaatgagcc aaaatgtaac 14760 taactgaatg tgtgatatgc acaatagcag ttttttttcc tgataatagg tattagttga 14820 tagctgcagt tgaaatagtc tgagactggg aaaggaaact tttcacattt aagtatgacc 14880 aagtttagta agttctaaga tgtttctgct tcagtagcag tgcaattgac ttttggaggg 14940 aggagaaaag cttctaaaat tattggtttc tacgtgttac tgtccactgg tgaaggtcag 15000 atttctttgg atattatcat gttttccagt aaactttgag aagtgtgctg cttcacaatt 15060 ttatcctaat tccctggggt aataattgaa aacttcataa acatattttt aaaattttct 15120 agatccttat gattgtttat atgcttaaaa aacttcatac tagatattaa tttaaagagg 15180 tcagtaaaac aaaatggtga actatgtgtc agtggaatca aactgtgaat catttctttg 15240 cccagtttcg ttaaaatatg tgatcatgtg agtctttaac tgtctgctga agatcagtgc 15300 agcaggccac agactgttaa atacatttct gcaatatatc gggggaggtc aatttcttaa 15360 tatctttgtt aaaaagtaga agacgcaagt aaactagatt tcatacatgt agtcttggtt 15420 ggtagtatct cctgaagcat gtggaggaaa attggtagat cgaaacagaa tgatagcatt 15480 cagagttctc agggagagaa ccgatttaat caaataaaat gggctttgca catttcggca 15540 agttcaagac actaagaaaa gcccttgggg aagtaacttt tataaaactg aatccaagag 15600 aactggtttt tcttttcttt tttttttttt tttttaaaat agagtcttgc tctgacaccc 15660 aggctagggt gtagtggcgt tatcgtagct cactgtagcc ttgaactcct gggttcaagc 15720 gattaccact tggggctaca aacacatgcc actatggttg gctaatttgt atgttaattt 15780 tttgtagaga gaggagtctc gctgtgttgc ccaggctgat cttgaactcg tgggctccag 15840 tgatcctctc tcctcagcct cccaaagtgt tgggattaca ggtgtgagcc actgcaccca 15900 gcctggctat cctttaaaaa gtaattttaa agctacacta tacatttaaa acacagaaca 15960 ctaaaatacc tcctttgagc gttgaagtat attagtacct tgagtaaagt gagaaaagca 16020 caaaaaaagt gaaatctggc caaattgttg gagtatcagg gaaaaagttg tgtcagggtc 16080 agaaaatata agcaagaagg aagtttttag gggaggtaca agaaggaaga cagttccatt 16140 cttataatga tataatgtat tcttagtgtg tactttataa ttgtaacaac ctcctttata 16200 ggtgtgctag ctgtaaaaat cattttacaa agatatttca acagtttaag gtgattcagc 16260 tgtcacagtg ttctgttacc taagagagca agtaaacctt gtctttgtta tcagaattgg 16320 agtccatttt aattgtgaga agaaaattcc tgaagttgag aagttttaac ttgcccaaat 16380 attcagggca aagaccaaga gaaaagtcat ttgtctcctc gggagacaga gatgattgga 16440 aaagcagggc ttcttatttt tcatgtcatt ccatctcact ggtgagttta ccaatgcagg 16500 aacagtttgt gatgacagag atgacagaat gctaagttga agaagaaagt gagttggttg 16560 aaaaatactg ttggaattga tttatgcaaa ttttctgggt tgtttcagag caagttttcc 16620 ccaaacttat ggagagcaga tggaaaaagg aaaatagttt atctttcaac aagagaaatg 16680 atggccctgc taaatttaga ctctggcttt aacttgtgac atctgggaaa atactcaaat 16740 ctgttaatca tttagtttgt ataaccacct agaagagccc aatgtccagg atagacctct 16800 aacatgggct tacaaatggc agatattacc aggctgattt aatttccttt aataaaagat 16860 aaaaagtctt gtcaaggaga ggaaagcaac atgcattggc tttctggatg tcaacaaggt 16920 tttccttcat tcattgtgaa gagcttgcta acaagctagg aagatttgga ctggactgca 16980 ctgctcctca ggggaatgtc cagataggct gcaggatgta tgtgcctaaa acaggtcagt 17040 gcagtggctc agcaccaagt cagggggaca ccacaaatgg agcctcccag caagaagttt 17100 tgtcactgct gtgtgaagga gcctggcttg tgaaaattca taacgtacaa ggattctttt 17160 tactgtttgg aaagattcat tgccagtccc tttaaatagc taccacccta gagaatatta 17220 atcattcaac tatttttttt tatttataaa tagtcaattc acatacagtt tgtaagggtt 17280 acttttcttg tggaaagtta ggtacagctg ccctaaatat ctttatcggt taccttggct 17340 ggggaaatta acagcatgtt tattaaactt gtacattata ctgtgttata acattatacc 17400 attttccaaa tattagtaag gtcgctaaca ttttggaaaa ggattacaag tgacctttag 17460 agatagaaca ggagtttttc agaaagggcc tctaacacca ctcccacatc cccttcgagg 17520 acagttgatc tgcttttatc tcttttactt gttcttagtt cctggcaaga tttcaatgga 17580 ggaaaaggct tctctattta aaaaaaataa aaatcaatga aaattaatga atcggagaaa 17640 tggcctggct aaaatgggat gaagttcagt attaggatac tgagggatac tgaagtttag 17700 gggagccact aaataacact ccttcatttc cctcctccac ttgaaatcta ttgagaggta 17760 agacacagaa gccagccaga gttccaaatt acagctttat tcctgatcaa agctggagga 17820 aaggatgtag cctacatgtg tgttctgaaa agcttccaag tagttcacat attgacagac 17880 ctaccctatg ggtctgttgt aggggtggaa cctacccctt tagcaccaca tgtcagagaa 17940 cataccagaa tattcaaaag agcttcagca acaggcctgc agagagcatg ccagtttcct 18000 gtttgcaaac caaccagtca gatgagaagg tggaaatgtg ggtgcagagg gtaatagaaa 18060 atattgcttt taggctttgc ccttctgagg agaaaagtgc aaattctctc cttcctgtgg 18120 tgatgtaagt ggagaataaa tagctagtgg ctagtcagat caagctggga caagaaccca 18180 ggtcactgat agaaaggccc atgtttttct gttggtatga aaagacattt ttagttgact 18240 atggaaactt aaacccgatc tgaattaaca tattgaatta acatttattg agacaggagg 18300 tgttctcttt ctgtaagtca gatttacatg aaggattgtt acagggtgta gaattataag 18360 atacataagt ctgatttata ttaaaggaac gtatagaatt ataggatata aaaactgcaa 18420 gggaccttag agttggtttt tcagcccttt cattccttgg gtgaggaaac agccacagtg 18480 ggattaagtg acttactcta gaccacttgc caagcgagtt agtgacagct aggaatagac 18540 taggcccttc taattcttaa ttcactgttc cccacaccta attgttctgt acttagatgt 18600 cagggaaagt aggcttaaat taaaatgaaa tttgaaaaat ttattaaact tataaactaa 18660 tctaacaaga catatttgtg aagtgaatat aggcttacca tgaagatagt gcaggttcaa 18720 ttcccagacc accacaatga agtgagtcac aagaattttt tgctttccca attcatggaa 18780 aaattatgtt tacactatac tgtagtctat taagtgtgca atagcattat gtctaaaaaa 18840 caatgtatac accttaattt aaaatacttt gttgctaaaa aaatgttagt gatcaactga 18900 gctttcagcc agtcataatc tttttgctgg tggacagtct tgccttgatg ttgatggctg 18960 ctgagtgatc agggcagttg ttgctgaagg atgggggtgg ctgtggnnnn nnnnnnnnnn 19020 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 19080 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 19140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 19200 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 19260 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnntcataa 19320 gaaacaactc attcattaaa gttttattat gagattgaag caattcagtc acatccttag 19380 cttcacttct aaatctagtt ctcatgctct ttctaccact tatgcagtta cttcctccac 19440 tggagttttg aaccccttaa agtcatccat gaaggttgga atcaccttct tccaaactcc 19500 tgctaatgtt gatattttga cctcctccca tgaatcacga atgttcttaa tgtcgtctag 19560 aatgttgaat cattcccaga aggttttcaa cttttcccag acgcatcaca ggaatcacta 19620 tctatggcag ctatagccct acaaaatgta cttcttaata gccttacaaa atgtattttt 19680 taaataataa gacttgaaag tcaaaatgac tccttcaccc acgggctgca gaatggatgt 19740 tgtgttagca ggcatgacaa caacattgat ctccttgtac atctacatca gggctcttgg 19800 gtggccaggt gcattgtcga tgatcaatag tattttgaaa tgaatctttt ttcctgagca 19860 ttaggtctca aaagaggggc ttaaaatatt cggtaaacca tgctgtaaac agatgtgctg 19920 tcatccaggt tttgttgttc cattgctaaa gcacaggcag agtagatgta gcataattct 19980 taagggccct tggattttca ggatggcaaa tgaatgttgg cttcagctta aagtcgccag 20040 ctgcattagc ctctaacaaa aagtcagcct gtcctttgag gctttgaagt caggcattga 20100 cttctccttt caaattatga aagtcctaga ttgcatcttc ttcctataga agtccgcttc 20160 atctacattg aaaatctgtt gtttagtgta gccaatctca tcagtgatct tagctagatc 20220 ttctggataa cttgctacag cttctatatc agcacctgct gcttcacctt gcacttttat 20280 gacatggaag tggctgcttc ttctagcttc aaagttttct tctgcagctt cctcacctct 20340 ctcagccttc atagagttga agattcattc catcaactct aggaagagtt agggccttgc 20400 tctggattag gctttggttt aagggaatgt tgtagctgat ttgatcttct atccagacca 20460 ctaagtcttt ctccatctcg gcaatgtggc tgtttttctt cttactcctg tgttttcctg 20520 aagtagcatt ttaaattttc ttcaagagct ttcctttgta ttcacaacgt ggctaactgg 20580 tgcaagaggc ctagctatct cagctttcga catgccttcc tcactaagtt taatcatttc 20640 tagcttttga tttaaagcga gagaagtgca actgttcctt tcacttgaac gcttaagagt 20700 ccattgtagg gtcactaatt ggcctgattt caatattgtt gtgtctcaag gaatagggag 20760 gcctgaggag agggagagag atagggaaca gctggtcgat ggagcagtta ggacacatac 20820 aacatttatc gattaagttc actgccctct tatgtgggta tggttcatgg tgccccaaaa 20880 taattacaat agtaacatca aagctcactg atcatagatc accataaaag atataataat 20940 aatgaaaaag ttagaaatat tgcaaaaatt accaaaatgt aacagagaaa cacaaagtga 21000 gcacatgctg ttggaaaaat ggcactgata atacagggct gccacaaaca ttcaatttgt 21060 aaaaaatgca atatctgtgt ggtgcaataa agcaaagcac cataaaatga ggaatgccaa 21120 tatacataat gtgtggaaga gtggtttaaa ttggtgggct ctgaagttag gctatctgga 21180 ttcaaatctt ggctgtgcca tttcctagtt gtctggcctg gacaagttac ctcgctttcc 21240 caagcctcag tatcctcatg tataaagtga agatagtaac agcacctacc cagagggtgg 21300 ttgtgaggtt catgtaagaa ggatgtatat tacatgctat gcttagtata agtgagttcc 21360 taacatataa gcactgataa atattagcta tcattagtca tcatcatgat tattttacct 21420 tggagagact taaaatttga cctgtgaaga taataaaccc ttagcttagg attctaccca 21480 tcctaagtta ctcctttgtc ctaaacctcc attctttagg cctcttgtaa tatcttttac 21540 tgtctatcct ttggcctcat gctctatcac caagtctgtc ctatttgttt cacatgtttc 21600 tcatttaact ctttcatctg catttccatc ctaattcagg tcttgattcc ccaggtgtgg 21660 cttactattc aagcctccta gctgctcctc ctcctcctcc tcctcctcct cttcctcccc 21720 ctcctcctcc cacccccttt tttttgagac agggcctggt tctgtcaccc aggctggagt 21780 gcagtggcat gatggagtgc agtggcatga tcatggcaca ctgcggcctc cacctcctgg 21840 gctcaagtga tcttcccgcc tcagccttct gagtagctgg gaccacaggt gcacatcacc 21900 atacccggct atttttgtgt gtgtgtattt ttggtagaga cagggtcttg ccatgttgcc 21960 taggctggtc tcgaactcct gagctcaagc aatgtgccgg ccttggcctc ccaaagtgtt 22020 gggattacag gtgtgagcca tcgcgcctgg cctcaaacct cctagcttct tctgactaca 22080 gcttcacttt cctgcaggct gtcctgtatg tcactatcag actgattttc ctgtttaccc 22140 ctgccttgga ttctgtagtg tgtctactgt ctgctgcttt aaggccaggc tctcatacct 22200 gaccttcagg tcttttagga acgtcagtgt ccaatagaaa tataatgtca gtcatacaca 22260 taatttaaaa atttctacta gccacattaa aaagtaaaaa caggtaaaat taattttact 22320 aaaatatttt atgtaaccaa aaatatccaa gacattatca tttcaacatg taatcaatac 22380 aaaaataatg agattttggc attttttgtt ctgcatcctc aaaatgccaa atgcattcta 22440 tacttacatc acatctcgat ccaaactagc cacacatcaa gtgttaaata accacatgta 22500 gataaaagcc actgtatcag atagtgcagc tgtagaatgt gacttgccac cacataaaca 22560 agacataact atgtttcact tcttccttgt ttgttaaaat agggatgtta atgccatgcc 22620 tattttatag ggttgtccta agccaatgtg aagtgtgaaa gtgctttgta agcagtaaag 22680 ttctgtaaga atgtatggaa gttattatca ggagtgaagg tttttactaa cataagaata 22740 caatatcttt ggagtaaagt aatttaaaag aaaaacccat attaaggagg caaattagct 22800 gtcctgaatt catttgtgaa aaaaattaac tctaagcaat gaatggagag tgtaaatgta 22860 tactcactat ctctttataa ttatcttttt ggtagaaatt tatcacatta ataagattct 22920 ctaaatactt caataaatct gtgggccttt tttccttcag catgttgagc aatggacata 22980 gggacatttg gttcttctct tgatataggg agctggaccc ctaccaaaga gttcattgct 23040 cttggtagta aatgtagcct acatactttg tagtactgag gtaggagtgg cattaaaatt 23100 tcccatatca tccaattcat tgcaaagaat aggaattaac ctacaaacaa tgtcagagat 23160 ttagatacag aaactattaa tatttgggcc gggcgcagtg gctcacacct gtaatcacag 23220 cactttagga ggccaaggca ggcagatcac ctgagctcag gagttcaaga ctgccctggg 23280 caacatggtg aaaccctgaa tatactaaaa tataaaaaat tagccaggca tggtggcaca 23340 cgcctgtagt cccagctact caggaggctg aggcacaaga atcgcttgaa cctgggaggt 23400 ggaggttgca gtgagccgag atcgtgccac tgcaccccag cttgggctac agagtgagac 23460 tccatctcaa aaaaaaggaa agaaaaagaa aaagagagag agagaaggag agaagggagg 23520 gaggggaagg aaggaaggaa ggaaggaaac tattaatatt tgtaaaatgc tttcatttca 23580 tattctgtat tctgacagat tggtgaatag caccactaac gataaggaca cattatttta 23640 aataaagatg agtcataaag tggtacccaa atcttatcct agccctttac caaaccaaat 23700 agtccactaa tttttaaaaa ttataccttg aactaccaca tggcccttca ggtgttcaaa 23760 tttaatatat aacctttgtt accagtgtgg aaataagatt gctaaacgaa gtgactccaa 23820 aaacaagaat caattttata taatggcttc agggtaaagg acccccgccc accatttaca 23880 agtttgccaa agccagaaac ttcaacataa tgcatgacct tttctttctc acctgtccct 23940 ctaattagct actaaatcct taggactcct cctctgaaat acttccttaa tctgcaacct 24000 cctctccatc cccactgccc taactcagcc tttcatcact tttctcgtaa gctctttcag 24060 cagtctccaa accagtttcc ctgcctcaag cttcagcctc ccctccaccc cacaatttat 24120 tctccaacta ccagcagaga tcttagtaaa ataaagatct gatcatacca ctccccggat 24180 ttaaaacctt gagttcttcc cagggccagc agataaaatc caaactgctg agcatggtgt 24240 acaaagcact ttatagtcag agcccaaatt atcttaatca gccttgcctc ctgccatgtg 24300 cccagagcaa tgataatcag attactggtg gttctcaagt aagtcctatc cttttatctg 24360 ttctcttccc ttgcacagtc ccctccaccc ctcacatcag tgagtctcat gatcttcact 24420 ccatcccatc agtatttctc aaatgtccca cttttcagtg agaagccttc cctcactctc 24480 tggtcacttg ttctttcagt ctccataagt gcatctctta ttcctttgtg gcaggaaccc 24540 ctcaagagct aattcctctc tatatcccca gcacgtagca ttctgccaag tatagcatag 24600 tttgtcagta aaaaatctgt tgaataaata catgaaaaaa ttgatcctct ccacccaaat 24660 gtacaccttt ctcttctacc ccaaagaaga aatctaattt cctaattcag tgtgatttat 24720 aatcaactac tgatagttcc aggtatttga aaagatactt taaatcataa tgcttccttt 24780 tcactaaagt tcagtttatc tagtccaata agattttcct tgggccataa agagttattc 24840 tcattcccta tatttccagt actaaaagtc atatatacaa tttggccaaa ggagcacctg 24900 gaaagtttta acctttaaat gcttcgacct ataggatatg ttaggaacat taaaataaaa 24960 gacaacaaac taagcacatc tttaatttca caagaattgc cagctattgg acctggagtg 25020 aatcttaacc aagatcacct tcaccttgaa gggttatgca ggttgtgttc tgtttaaccc 25080 tagggggcgc cactctcaca gattatgatg tgaatgactg caaggtggta tcattctcag 25140 ccttatacag tgtccctgct tatcagatca tcctcctttt cagcttaggt cctaagaagc 25200 caactggttt gctcaaggtc acacaggtat ttcataacag ggttcatagc caataacctg 25260 ccccctttct tacttcccag tcattctact aatccaaatt gctctggaag accatgaaac 25320 cagaaaagag tgtttgatgt agttgcatgg ataatggact atatgccttc agctaaatgt 25380 gaaattcaaa tggtttggtt tatctcggta tcatttgctc ttgttttcca cctctagctg 25440 tactggcctg gttggcataa cttcagcatt tagcatatca cactgctgct ctcaggctca 25500 ccgagactca agtggctgtt ccactctgtt gccacgctgt gctgtcttct ctctttcttg 25560 ctggcccatt cctctgtgac ttcctgttag ctgccacctt cttcttttag cttctcttct 25620 cagcactttt tgctgctttg tttttatacc catctcagac cagtcagcac gatcctttcc 25680 ttccttctat tctacaaacc aatcaatcac agcatgttgg ctgttgacct tggatctttg 25740 gttgtttgct gctgttcata gctgctgggc gtggctaggg gatgctgctt ctttgccaaa 25800 actttttgtt tctttttctt tctcccttta ttctagatct tgggctttct gaatgcttga 25860 agataccaga agggttatat ccaaataagt gtggctctat tcctattact ccctctttac 25920 tcttgcttaa aagtgaaaat attgcttcgg tggaagaatc ttggttagaa gaattaatgt 25980 agctcagaca gtcaatatag ctaattgtct ttaccaagga caatgcattt aaaaaataac 26040 tactccttcc tctgcccctt actcccatgc tcaccatcaa tgtgaagcta gggtaacagg 26100 tgtgttggca ggtttggttg agcctgaaca gaaaactgga cctcttgagc cacagtcctt 26160 cagccataat ggacgaagta ttttttgctt cagttctttg cgcttgatca ttagagctag 26220 caggtctttc cgaaactgct tgctttagtt ctacctgatc agtgaagata tagaatagaa 26280 ttaggttaaa gagtggttaa tttcttagag ttttgatact tgctgtttag tgattgtact 26340 ttatatattg ttcattgtat aatcaagaaa ttctttgtaa atgtttggtt tgcaggctgg 26400 ttggaaggaa aatcatgcaa cattcatgag cgaactaaaa aatcttcagg cttctggact 26460 gactactctc ggtcaggctc taagatcctc atttgatttg ttaaatctca atagattaat 26520 atctggaata gacaattatg gacaggtaaa aataatttga gtgagtacag ctaatttatt 26580 ttggtggctt ggggtaagaa tttaaaattg ggcatgatta ctaagttttc tgctactttt 26640 cataacctcc aaaaatgaga ttcttattac cttttaaata tatacttttt aaaaatccct 26700 cttcttttgg ttcttgtata tggcttgata atagaatagc taaaattgtc taccatgaga 26760 taatcagatg tttgagaatg atgtgaataa acggctgaga aatatcggaa caagacaatt 26820 ggaaagaaac tttcagtgtc cttaactcct ctgcccctcc caatttgatg aaaaagctct 26880 aggataagaa ggcagagtag catttgctgt tgctcccatt gtcctttcct cctctaaagt 26940 ctgtgctcac agtaaccaga gtcactctcc aggttgcagc acgcaagtca ctagtgtcct 27000 atctgtgcca ggattttgac ttaagtgaat ggattcatga gagtggatga taatgccagt 27060 aatcttgtaa tattattttg tgattacttg gaaagcagag tgagagaggt atttgaatgt 27120 taatggtttg gggagttcct gaattataag aattcctcag tttatactga atgttacctc 27180 ttcaggggtt gttattttta ttcctaccca tttcgttccc tggtcatttc ttccttattt 27240 atccagacaa attttatcat attcttgaga gatcattggc aaggcaaata taaaaattta 27300 aatatacttt tattacttta catggctcta atgcttttta aatgtatttt aggggagaaa 27360 tccatttttt ttagaaccat ctattttaat taccatcaca gatggaaaca agttaacaag 27420 tactgctggt gttcaagaag aggtgagatt ttattttttt tttaattttg tttaaatggc 27480 agggaacatg cagctatttc tgtgggaggc atttccagtt aacagtaagt ttggtcaaat 27540 catccatctt ggtaatcctt gaaagactgc ttaattttat tgagttacat gaaagaaaaa 27600 gtcaaccctt taattctttc ttcattttta tatggtttgt tatgatgaac cttttcacat 27660 ttttgcctta tcagctccat cttcctttga attcccctct gcctggaagt gaactaacca 27720 aagaaccttt tcgttgggat caaaggttat ttgccctggt gttgcgtttg cctggagtgg 27780 cttctacccg aaccagagca actagggagc gtaccaactg atgaatctgc catcacacag 27840 aatgtgtgaa gtcacaggag gtattggcaa tatttaatgt ttctgaagga aaaattcaga 27900 gcatagagta tatttttcat taaatgccat atccagtctt tacttgtttt ccttcaaagc 27960 cttttaactc tgttgcttaa ggtcatcatt ggtatatttg ctgccaatgt agttatgatt 28020 atttcaagtt atattttagg attttaaaat gcttatatta tgaaattata tttgatcaaa 28080 cttgtgctat ttatttttcc ttctgggata ggtcgctcct actgtgtgag aacacaaaga 28140 atgttgaatc aatgtttaga atctctagtt caaaaagttc agagtggtgt agttattaat 28200 tttgaaaaaa caggaccaga tccacttcct attggagaag gtatagtaga taactttttt 28260 aaccctaaag tgttatatag gagaatgaga agacattaaa taaattacta tagacacagt 28320 cttcactatc cacgtgcatt tgagtggtta caaacataca tccaaacaac taccacacat 28380 tcactgccta tgtatatgta tcaggtggcc aaattctaac aactttaatt tcatgttgaa 28440 tgttcctaag aacgtgtttc cttttcctgg tgcattttat attccctggt cccagtcttt 28500 ggatggcact gactcattca cctctctatt cacaaaatgt ctggagattc actatggtgt 28560 acacttaaat aataatcttg ttttggtttt gtgagtgcca aatatgctaa gccatcttta 28620 cgaaatatgt gttagtttct gcacctcagc aagaaattat gaatgtttat ccaggaactg 28680 ctcatcttct ctaagatcct acactagtat tttcccggtc actttttcac tctgaagtta 28740 agagttgagc aaccttttct ccaaatgaga tttcacagaa agttcgacat ccaaaacttg 28800 atgaaagtag ggtgactttt gcatagggga agttaaatcg tagtgaatct ctagatggtt 28860 tgtgaatgga tgtttgtaat cacttgaatg caaatgaatt tcaaagggat cagggaacta 28920 aacaagcacc atggcaacgc attgcaagac ttccatggta atgcactgca agaacagagc 28980 tcctagaaag tctatgtgta tatgtatgta aatttgtaag tgtatatata tatatatata 29040 cacacacaca ctccattatt attaccacag tgattgtcta gcctgattta tatgttttaa 29100 ttgccttgac gaagaacaaa ggggtcaaat gcataagggc agaaagctac acatttctgt 29160 ctgaagcagt ggatcctgtg gctcctgatc ttttgttgtt gttgttattg ttgttgtttt 29220 gctctttagt tccccatcct tttgagaagc tgttggaaaa aatatagacc ccttttccct 29280 ataaatacag acataagtga cacatttcac aattttgtat ataatctcag gggttttttg 29340 ggcctccaag ttaagaacat cttgccataa aagactgagg gccccacagc ctattttaaa 29400 ttaactgtgt aggaaggcca tgttatactg ctagcaatcc aaaatttcgt gctcactatc 29460 ttagcataaa ctgggaactt acatattgaa attctagtag gatttggtgt catgtaaatg 29520 gcacagattt tttttctagc tccagttctc ctttgtccag agttcttaac ctttcaggtt 29580 ctgatgaaag ttaagaaccc ttttcctcag aaaaatgcac attgtcagaa ttgtgagctc 29640 aactttgggg ggatcctcca aagccattac actttttttc cctactgcac agtggaccca 29700 ttaaatctcc tagtctaaag aaattacttg tttaaagtaa tgcttaaata agttattcaa 29760 atgactgata atttaagaaa aatgagactc aaatcattaa agcatatctt ttacaaatat 29820 tatcattaaa agtttatata actctgcctt gccctgattt gaggcggggg gagaaggagg 29880 aaggaaatga aatatgctag tttaaatcat taaaatgcat tcaggataca ttattcagca 29940 ttatacaaca cccattgtcc atggaatttt gatggtggat ggagaaacca tagtgaatta 30000 gtccacgata aacttgatgt gtttgctttg tgctcccctc aactatatac acattgtctg 30060 catttcttct atctttaagt gaatttggct agtttttatt ttgcctttgt ggtcattggg 30120 tctaattgtt tggcaaagaa cacttttttc ttgtatttgg aaatagaaag aatatataaa 30180 tggaatttat gatctatttt tgtcagactc cagaaatgta aaaactatac cagggagtga 30240 acaatttcat ttgcctaatt tagtaattga attcttgaaa aataactgta gtgttttgat 30300 gtttttaatt tatgtgtacg agtctcagaa aatttaaaac tagttttacc atagttttct 30360 gcataactgc atattctctt actaggttaa gaatggtggg gtgggtgttg ggttagaaga 30420 gatggattag acgaaaagag ttgctagaga gaacatttag aaatcctagt agagtcactt 30480 ttttttcttc ttccattttt catgaatcat tgttcttgtt ttattttgga ctttgctttc 30540 agctggaaaa tttgtacaag aagatcagca gctgtaaaaa gaaactcacg ccttagtttg 30600 tcttttgttt aacttttaga tggacttatg gattcatcca ggccaagcaa ttcatttgct 30660 gctcagccat ggcatagttg tcataaactc atttatgtac gacctaactc taaaactggt 30720 gttcctgttg gacattggcc aattccagaa tctttttggc cagatcagaa tttaccttca 30780 ctagtaagtg tcataaaata aaaaggtaaa catcattctg gattttcaat tttctgatta 30840 cagtgaacct tttaaaatag ctttgaggcc tttatgccat gccacaggca agtaagtctt 30900 ccctcctttg ccttctgtct cttacctggg aagtctagct ttgtgcctaa aagcaaaggg 30960 aggacttcct ttattttctg atacttgtca ttcttcagtt gccttcgcca cttgagctgc 31020 cctttttgga tgttaaaaca ttgctgtttt tgatgctgtt ataatctgtt acttggtttt 31080 catttcagag cagctgactt gatttacgtg gcaaacacaa cgtctaaaat gtactggcct 31140 tggttttcat gcacagcctc aggaagtttg aacatagttt acaccttgga taggttctgg 31200 gaacatatta aaatcatatt caaaattcta cttcttccta cttttcatct ttttgtaatc 31260 aatggacttt tgtagcaata tacctttcaa tgatgggtaa ttaagcaata tttaaaaaat 31320 aatctctaag caaggacttg tctttttggt cactgcattt ggtaggagag gctttgctat 31380 tacagttgct cccagtgcca gatcaattgg cttttttttt ttttttttgg agggagggca 31440 gtgtctagta ataaaggaga cggtatgaaa cccactctct tttgtcttct ttccccttcc 31500 ccaaattgta agagggcctg agtaatctcc cttgtgtggg ctcaggaggg gacacaaaca 31560 aatcactact tcttctattt aacatcttcc tagttcagtt catctatatt ctgtctcagt 31620 tttagaaatt tctgacagtg aattgcattt tctcctggat tactgctttt aggcttctgc 31680 ccttttttca gaagtggcca tgaaagacct gaatgtaaga ctgaagagcc cttttggccc 31740 ctgctgtggg tgagggtaaa cgtcccactc ctctcctcag ggcttcaagg tgttacacct 31800 gtgaaacctc agcccttcca aactcgagta caggctttat ggcaaattta cttcattttt 31860 gctagcaaca agtcttcatt catgtcttta tgacattttt acctgttcaa atctaaggag 31920 tcagaaacct ttcacaagtt aattaaaact aagttgggaa aaaacaaaat agaataagac 31980 attccaagta attcacacat agctcatgtt accattcctc catctttaaa agttcattta 32040 agagctattt ttctcaaccc ccaaacatct tataattgta aactataaag gcaagtgaat 32100 atgttttcat tttttataaa ggaagcagtg atattttatc atattcatat tagctttaca 32160 ggtttcgcaa caagaatagg ctgacccact tcttactttg tcttctggga cttgtcctgt 32220 gtccctctct ctccatattg cccttgctgt tcgcctttct ctctctggtg ctctccaatc 32280 acacaagcta aacctgttac ttaaatggct tctccattaa tctgctccag caccccaggt 32340 acacaggcct tcgaagccca gcgcaaagnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 32400 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 32460 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn tcaacattca tcctacaatc ataagcactt 32520 cttaaacata ttcaaaacag ttttttttca attcactgaa attttagtta tgagtgttga 32580 aatttacctt tcctcttcct aatgtcaagt agatagtaaa gaatctgagc cctctctccc 32640 atggaagcca ttggtggttc ctagagatct agtaatcttc tttctcaaaa tgctagtctg 32700 tatttcagtg aaaatgtaac aaaatataaa acgacttgca gaattgtcag aaatataagc 32760 ttgctttgag acctaaccat tttttctgct ttttttaaaa aatttttttt agcctccacg 32820 aacatctcat cctgttgtga ggttctcctg tgtagattgt gagccaatgg taatagacaa 32880 acttcctttt gacaaatatg aacttgaacc ttcgccctta actcagtata tcttggaacg 32940 aaagtctccc catacctgct ggcaggtact tatccttacc tattagctaa atgtctgtaa 33000 ccactctagg atctgggaat tgttttaaga agcttcaaag gttattctca aaataattgg 33060 actgactgtg ctaatgatgt ttctcatgaa tgctgtcaaa taagcaacag ggccaggcaa 33120 ataatttcag actaatatga atcattagtc tactgtacat tgccatttaa agcaatagag 33180 tctgatgaaa cctatatatt tgaagatttg ggggacccct tgaagtctac ccatgcaccc 33240 cagcttaaga atccctaatc taaaggttgt acttcacttc aggtatggcg tctgcagctg 33300 aaacaaggtg tttagccctt actttgaact tgacagattg gaagtacagg atagtttagg 33360 cagagaacca taagtcctga aactaatttc tgtattagtg taatataata aaactcttcg 33420 tcctgtggta caaatcacac taaaaaatgt gtgtaatgtg gattttgcaa cttggatgag 33480 acaaatgcat agagatatct atcatacact ggctcttcca agtgttacac ttaagccaga 33540 aggatttgct gattggttaa tagagtcacc tatggaattt aatttgtaaa aattcagaga 33600 tggcagtcac agccttttta tgtggataca acaaaaatgt cctacactgt aaagatgtat 33660 gttctatttc taaactgtag agatgtatgt tctacttcta ttaatatata ggactctata 33720 gcaatcagta actgttaggc tctatttatg caaggaacac tttcagactg ccatctgttt 33780 tatcttaaaa tgtgagatta ttgctacaag ttgtctgtaa gctacttaaa ttctcccaag 33840 atgctacaac tagttagaaa aaaaggagca ggattaaagc aagaatgtaa aagcacaaga 33900 aacagaataa tctcacaaac ataatactga gcaaagaagc tagacagaaa agattacata 33960 ttgtgtgatt ctatgttata tactttcaga gagagataaa actaacttac tctgttagaa 34020 gtcgggatag tggtttctct tggggggatg caaggtagtg gacagaagag gacacaagga 34080 gatgtctggt tttgttctct ttctttcttt cattcttttt gttttgtttt gttttgagac 34140 agcgtccagc ctgttgccca gggtggagtg cagtaacaca atctcagctc actgtagcct 34200 cgacctcctt ggctcaagca aagcgatcct cccacctcag ccccccacag aggagctagg 34260 actacaggca cacaccacaa ttcctggcta attttttaaa tctttttttt tttttttttt 34320 ttttagagag acggagtctc accgtgttgc ccaggctggt ctcaaactcc tgggctcaag 34380 caatcctccc acctcggctt cccagagtgc cgggatgatg gcatcaacca ttgtgcctgg 34440 ccatattctg ttttttgact cgtgtgctgt ttacacatgt acattcactt tgtgagcatt 34500 cattgagctc tatacttata gtttacccca aaagtgctag aaatgtagag atatggataa 34560 tagattgcta atttaaaata aagatatgac ctttgaattt atgggttgaa aaacattttt 34620 ataatgaaag caaataaaat tacaaattat agcttttccc taaaataacc cctcttttct 34680 atatagcaca tttcttggaa accttcttca gagaaactta agaaatgctg tccttgctcc 34740 tgcactaccc cttaaatatg tcatatgcct ctttcctgta ctttatgtta ctttttttag 34800 agtattctta atgtgatgaa ttagtgttag tgaaaaagaa taaaatgaac cagtagccag 34860 gaaatttggc aaaaccacaa tggagaccgg agcctaaccc tagctctgtc accaactatg 34920 tggccttgca cgagggactt acattgtctg aactagctct aaagatcctt tggaacccta 34980 aaaatctatg aatctgtggc tgataaggaa tttggaaaaa ctcaaggggc caaggaaggt 35040 aggaaagaga aagagagaaa gaaacaaaat tcagtgcttt tcctttcatg ggaatcatag 35100 atctgaccct tgactgcctt gtgcatgtga ttttttttat ctttctttga tgaatttttc 35160 ctctcttcta atatacacac ttaggaaata aaatccagca tggtttattg cagttatctg 35220 tttctattat cattcaaatt atgacacaaa atctagtaga ctcatgtttt agtacaactc 35280 atgttctgtg gggtcataaa ttacataaat tacattacat aattatacca acttattctt 35340 agtgataata ttataagaag gtagtgaatt ggtaggtgat attggtagta ctgagaacta 35400 gcaaggtaaa tggattctgt taaatgtcaa ggttcgactt tgttgtaaat gattctgcca 35460 aaggactttg gaaaagtaaa ggaccaggtc tctaaaagta tatattggtg gtttggacca 35520 aagactctga acatggaaca gagaaaacat ggcagctagg ggaccccagt acaacatatc 35580 aactgtaagg gggctgatga tacaggaatc acatcaggaa atcaataagg agtaagaaaa 35640 tagtcatatg gaattaagat caatgtttta atcttcactg aatgtttact ctaccagcat 35700 aacttttttt tttttttttt tttttttttt tgagacagag tcctgctctg ttgcccaggc 35760 tggagtgcag tggcacaatc tcagctcact gcaacctcca cctcctgggt tcaagtgatt 35820 ctgctgccca gcctcttgag tagctgggat tacaggcgca ccactatgcc tggctaattt 35880 ttgtattttt tagtagagat ggggtttcac catgttggcc aggctggtct ggaactcctg 35940 acctcaggtg atccgcccgc ctcggcctcc cgaagtgcta ggattatagg cgtgagccac 36000 cgcactcagc cactaccagc ataatttata agagaaatgc cttccaggtt gacccaaagt 36060 atctccttgc tgcctcaaaa taattagcac cagtgcctgg cttattataa caggttactc 36120 agtaaatatt tattgaaaaa aaaatggata aatgggtagg ggaaggaggc agcaaagatg 36180 catggagcaa agacttaata atagtacaat gaagatggtt tacataatcc tttaagtagg 36240 ctttgttttt gtaatttcat gcttcaggca tgggactgtg ttctattttc ttcacagtct 36300 gcactctgat taccacttgt tcttttgaga agttaatttg ttttagtggc tggtttcctc 36360 ttagcagtat ttcagcttta tttttcattt tgctaagtaa gtaaatattt gggtactgtt 36420 gatgtggcct gtggtctctg aatggttgtt gcatagtata gtttcatttc ttaatataat 36480 ttataggaga attgcgatct gaacattcat atttagtagg attttttttg agacagggtc 36540 tcgctctgtc acccagggtg gagcgcagtg gcacagtcat gactcactgc agcctcaagc 36600 tccctggctc aagccatcct cctgctcagc ctcccaaggg atctggggac catagggcac 36660 gtgccaccac acttggctaa ttttttaaat ttgttgtaga gaatgagtat ctccctttgt 36720 ctcccaggct ggtctcaaac tcctggcctc aagcaatcct tccacctcag tctcccaaag 36780 tgtcaggatt ataagtgtga gccacctgta atcctagtac atgagcctgg cctagtataa 36840 tatattttga cataaccata ggctaaaaac actattgcta ttttaaaatt acaatcaaat 36900 tgcgccatag atgctgctat ggaatgttac aatgggtttg gtttgacata aaatccttat 36960 tgtcatcact gtgcattact tcatgttatt ctcaggtatt tgttactagc agtggaaagt 37020 acaatgaact tggatatcca tttggttatt taaaagccag tacaacttta acttgtgtaa 37080 acctctttgt gatgccttac aactacccag ttttacttcc tcttttaggt aagtaaaaca 37140 tgtgccactg aatcatcttt aaaatacaac agaaatgaaa aatcgataat agactaagca 37200 ttttaaatgt agatgacggt aacaaattga tttgaaagga tagaatttgc atactgtttt 37260 ctgttttgtt tgttttcttt ttgttgtttt tacatcaaac agaagagaag cttgactttc 37320 agtgtgtgat tcttatgctt gttcttcagg ttgcaacttc caatgcacac cccaccccca 37380 atccccagtt tgaagtgcac ttggcttttt tgtatagttt gggccaaaaa ataccaaaac 37440 agagctacca tggggtggga gtaatggctt gtgcttgttt cccctcagaa gataaatgct 37500 cttgaggcat ctgttttagg cagagtagtg agttaagaaa ataggtacca gagtaaattc 37560 tgcaatgact gtggttgtag aagctgtgat ttccatagca aggttctaaa aggaacaact 37620 caagaagctg ttactcagat actaatgaaa atgtgtgtgg agatattttc cccttattgg 37680 aagagccaca tctgtttaga gtaatgtagt acttactgca cagtatccta gttgtaaagt 37740 tgtaaatgtt tttatttcgt ggagtttctt aatttttgca aaaagggtcg aatctttact 37800 aagttttcat acgatcatta aaactatgag acttttagtg ctataaatac aacatacatt 37860 gaatatactg aaattgcaat acttttacat gtcgatttaa gaagtttaag aatgagtcat 37920 cgtaaatgta ttagcatgat tattttaaat aacctatcta ctttatttct tagtgcaacc 37980 taagagggat gttctctttc taagagctga ttatcattaa cataagatat aggttatatc 38040 tttcagatta ataagacagc cagtaaaaaa gtgtctgtat tttgcagatt tatttatccc 38100 ttttcttaaa taagtcttta tgacttcagt ttccacaact ataaagtgaa gagattagac 38160 tatgtaatct tcactaccac tgttaatgat attatttttc tatttttaag tgcacttttt 38220 ttgatctact ttattgagtt atgcttgacg tacaaaaagc tgtacatatt taatgtatac 38280 aacttgatga gtttggagat aagtatatac gcattaaacc atcacctcat tctatgccat 38340 aaacctatca gtcacctcca gaagtttcct cctgccctgg taagatctac cctcttactg 38400 accttttaag tacacaatac agtattgtta actgtaggta ctatgctaga aaacattatg 38460 ctgagtgaaa taaggcagac acagaagaac agataccaca tgataccact tacacacttt 38520 ttattttgag ataattgcag attcacatgt agttgtaaga aataatatag aaagagatga 38580 cctcaaaagc acaggctgca aagacaaaac tagacacatg ggactatatc aaccttaaaa 38640 gcttgtgcat caagggagac gattaacaga gtgaaaaggc aacctatgga ataggagaaa 38700 acatttgcaa atcatatatc ttataagggc ttaatttcca aaaaatataa ggaagtctta 38760 catttcaata gcaaaacaaa aacaaaaccc taaatagcct gcttaaaaaa tgggcaaagg 38820 acttgaatag atatttctcc aaggaagagg tacaaatggt taacaagcat atcaagagat 38880 gctcaacatc actaatcatt acagaaatgc aaatcaaaac tacagtaagg cattacatta 38940 cacccctcag gatggtcact atcacaaaaa cagaaaatga gaagtgttgg taaagatgtg 39000 gagaaatcgg aattcttgtg cactcttagg aatgtaaaat ggtgtaacca gtatggaaaa 39060 cagatagaag tacctcaaaa aattaaaaat aaaattaacc atatgatcca gcaatcccat 39120 ttctgagtat atatccaaaa gaatcgaatc cagaatcttg aagatatatt tgcacaccca 39180 tgttcactgc agcattattc acaatagcca aaaaaaaatc cattgatgga taaatgaata 39240 aagaaaatgt ggtagatata catgcaatgg aatattattt agccttaaga aggaaatttt 39300 gtgacatgct acaatatgga tgaacctagt ggacttatgc taagtgaaat aagccaaatg 39360 acaaatattg tatgattcca cttacatgag gtattaaaag tagtcaaact catagaaaca 39420 ggggctgtgt gaggggaaaa tgggaacttg ttacttcagt gggtaataga gtttcagttt 39480 tgtaaggtga aaagnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39540 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39600 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39660 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39720 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39780 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39840 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39900 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 39960 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40020 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40080 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40200 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40260 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 40320 nnnnnnnnnn nnnnnnnnnn nnnnnnntag ttatttaaga aaatagccta aatgtttccc 40380 agagtagcta tactatttta cattccccac tattaagtgt atgagtgaat cagtttctct 40440 gcatcttcat cagccattgg tgttgtcagt atttttaaaa ttttagccat tttgataggt 40500 gtatggtgat atagcactgt ggttttaatt tgtatttccc taatggctaa caatattgat 40560 catcctttct atgtgctgat gtgatgatgt gccattgtat atgttctttg gtgaactgac 40620 ttttccctat attttaatta gattgtttgc ttttgttact gttgagtttt gaaagttctt 40680 tatatatcat agatactagc cctctgacag ataggtgact tgcaaatact tatttagatc 40740 ttttttgatc tttcattggt gttacgcagt tttccactta caaatacggt gcatattttg 40800 ttatatttac acttacttca ttttttgagt gattgcaaat ggtattgtat ttttgatgtt 40860 ggtatctaca tgttcactgc tagtatatac aaatacagtt gatttttatg ttaatattgt 40920 atcctgcaac tttactgagc tcacttatta gttgtaggag agttttgtag attccctgga 40980 attttcaaca tagacaatta tgtcatctgc aaatagagac agttttacct ttcctattct 41040 tatctttatg ttttttcttt tcttttcttg ccttactgta ctgtagagaa cttccagcac 41100 tgtgtttaat ggcagtggta agatgtatgt tccatcggtg cttgacaact atgcactatt 41160 cattcttaca ttaagcataa tgcttttgta gattttcttc atcaagttga agagttctgg 41220 ctgggtgcgg tggctcacgc ctgtaatctc agcaatttgg gaagccaagg cgggtggatc 41280 acctgaggtc aggagtttga gaccagcctg accaacatgg caaaaccctg tctctactaa 41340 aaaatacaaa aattagctgg gcgtggtggc acgcacctgt agttcccagc tacttgggag 41400 gctgaggcgg gagaatcgct cgaacccggg aggtnnnnnn nnnnnnnnnn nnnnnnnnnn 41460 nnnnnnnnnn nnnnnnnnnn nnnncactgc aacctccacc tcctgggttc aagcgattct 41520 catgcctcag cctcccaagt agctggatta caggcatgta ccaccctgcc tggctaattt 41580 tcatattttt agttagagac ggggtttcac catgttgggc aagctgatct tgaactcctg 41640 acctcaggtg atccattcgc ctcggccttc caaagtgctg ggattatagg cacaagccac 41700 tgggccaggc ctcaaatgtt ctttctgcat catttgatat gaccatatga tttttcttct 41760 ttagtctgtt aagtatgatg gattacactg actaattttc aaatattgaa ccagctttct 41820 atccctgaaa taaatctcac ttggtcatgg catataattc ttttcatata tattactgag 41880 ttctatgtgc tgatattttc ttgagtaatt ttgtgtctat attcatgaaa gatattggcc 41940 tgtagttttc ttttttgttg ttgtctttgg ttttagtatc aaggtaatac aagctcttca 42000 taaaatgaat tgggaagtgc ttctcctatt ctgttttctg gaaaagattg tgtataattg 42060 gtattaatta ttctgtaaac atttgataga attcctgagt gaaactatct ggttctaaac 42120 attcctgttg ggagttttca aattattaat tcaatttctt tcatagttat agggttattc 42180 aaattatgta tttcattgag tgaaatgtgg ttatatgtcc ttttgaggaa tcagtccatt 42240 tgtccatttt atctaagttg tgaaatgtat gtgtgtagag tcattcttag caatccctta 42300 tggtcctttt gatgtgtaca gagtctttag tgatatcacc tatattattc ctggtattga 42360 taatacgggt cttatgtctt ctttgtcttt gtcagccttg ctagatgttt gtcactttta 42420 ttaatctcat caaagaacca gctgtttcat taatcttatc aatttttttt ttaaatttca 42480 ttgatttatt tcctttcttc ttactttaag tttgttttgc ttttcttttt tgattcttgg 42540 tatgggatct tagattattg gtttgatact tttcctcttt tctattgtaa gtagtactca 42600 gtgccttaaa tttctctcag cgctaattta gctgctttcc gcaaatttta catgttgtcc 42660 ttcattttca ttcactttac tttgtctttt gatttctcct gagacttatt tgacccatag 42720 attatttaga agtgtattgt ttgatttcca agtattttga aatttaccta ttatcttttt 42780 gttactagtt tctagattga attccatcgt ggtcagagga cacatctgta ttcgatatct 42840 actcttataa atatgttgcc atttgcttta tggcaaagca tattttctat cttaatatat 42900 attccagcag tgcttgagaa taatgtatgg tctcatgttg tttggtagga tattctacaa 42960 gtgttaaatt gttcctgttg gttgatggtg ttctgctata tccttgttga ttttctgtct 43020 atttgctcta tcagtttttg agagagggtt gttgaagtct ccaactataa ttgtggattt 43080 gtctgtttct ttttcagttc catcaatttt tgcttcaact attttgcagc ttttacttgg 43140 ttcatacaca tttagaatca tggtgtattc ttccttgatt gatcattatg taatgtatct 43200 ttgctaattt tctttgcttt taagtctgct ttatcagata ctaatgtatc cacttctgtt 43260 tttctttgat gtttgcatga tatatctttt cccatcattt tactttgaac ttgcctataa 43320 ctgttttgtt taagtgagtt tcttatggac agcacatttt tgggtcatgt tttttaatcc 43380 actctgccaa tctttgtttt ctaattgatg tatttagata tctgcattta atgtgattat 43440 tgttatgtta gggcttaagt atgccatctt atagtattgt tttctctttg ttctattttt 43500 cttttctctg ttttcatttt actggcatct tttgggttat ttaaacgttt tttagaattc 43560 tattttcttt tactatagta ctttcaagta tatctgtttg gatagctttt ttagtgattg 43620 ctccaggtgt tattatacac aaattaccac agtctactcg ttctcattat tttactaatt 43680 tgagtggaat atagaaactt tatctctcat tatattccct taccctcctc tatttataat 43740 aaaattatct gaactatttt atgtacaatt agaaatacat gaggcagtgt tataactttc 43800 gcttcaactg tcaaacataa tttagaaaac tcaggatgaa agtccattgt tttaaaccat 43860 attttggcat atcctgttct ttcttcctga taattcaagg tttgttcttt tatgtttaat 43920 ttctgtttaa agaacatcct ttagctgttt tttaagggta ggtctgctag tgacaaattc 43980 tcttagtttc tcttcatctg agaatatctt gatttcccct tcattcctga aatatatata 44040 tacatatata tatatgtata tacatatgta tatatccata tgtgtgtgtg tgtgtgtgta 44100 tatatatata tatatagcta ggtatagaat tctcggttga cagtactttt attttagcac 44160 tagaaaaatg ctgtgtaact gccttctgtt cttttggttt ctaatgagaa atctacttta 44220 attctaattg ttcttcctct gtaagtgagg tattgttttt ctttgctttc aagatttatt 44280 tctgcctgta gttttcagaa gtttgattat gatgtgtctt ggcatgcact cctctgagat 44340 tattctgttt gaggttcatt cagcttcttg aatctgtagg tttatttctc cttccaaatt 44400 tggccggttt tcagccatta ttaccttgag tactttttca gccccacttt ctttctcttc 44460 tccttccagg attctgttga catgaatgtt agatcttttc ttatagtctc ttaggttcct 44520 taggctccgt tcattttttt cattctattt tctctgttat tcagattggg taatttacat 44580 tgttctattt tccagttcat tgattatttc ctctgtcccc tgcattctgt tgttgagcct 44640 atctactgag ctttttattt tggttattgt atttttttaa ttctaaaatt tccacttagt 44700 tattctttat atcttctatt cttattctct gtttctttgc atgtgttttc atttgtttca 44760 agcctgctca tattattttt tgaaacatgt tttatgatgg ccgctttaaa ttggatattt 44820 ttaacatctc tattatcttg gtgttggcat cccttaattg tctttttaaa ttaattttga 44880 ggccaggcac ggtggctcac accttaatca cagcactttg ggaggccaag gcaggtggat 44940 cacttgaggt taagagttcc agaccagact agcctggcca acatggtgaa accccgtctc 45000 tactaaaaat acaaaaatta gccaggcatg gtggtgcacg cctgtaattc ccactactcg 45060 ggaggctgag gcacgacact tacttgaact tgggagacaa aggttgtagt gagcccagat 45120 cacgccactg cactccagcc tgggtgttgg agtgatacac tgtctcaaaa aaaaaaaaaa 45180 aattaatttt gagatctttc ctggttcttg gtatgatgag tgattttttt cctgtacatt 45240 ttcaatattt tgttatgagt ctctggatct tacttaaacc ttctgtttta acttacttcc 45300 tctcacaccc ctcttggaga aactgggagg tgctgcctca ttcatgccag gtagaagtcc 45360 aggctcgcca cttggccttc attgacacca aaagggaggg atctcccttg ttattgttgt 45420 gtgtgagtag gagttctgga tcctccctag aatgatacct tcctggctgg aagagatagg 45480 aatgcttcat tatcttccac acttgacctc cactgacacc atatgggtag aggtgacctc 45540 attactactg agcagttgtg aaagtcctat acaactatta tgggctaagc tctagggtcc 45600 catctttggt ctaaatccag cctgccttcc aaattattcc ctgaaaattc ctttaactag 45660 agtagctggt cttccagtag ctatcaggat gtagagcact ttacaatagc aagactcatc 45720 ctctcatctt tgcctttgct cgtctttcag gtaatggagg tcagatgaag gcatgacata 45780 atggttaaga ggaatgatta tagtgtgatc aagcattcag ttctcccttt gcctaaaacc 45840 ttctgtgctt aagttgccat gtggtgccct tccccaaact cctcagcact atgccaagtc 45900 aaatcctgac actgtcttcc tggtcacctt ttagtttgca tcactctatt cctcaaatgt 45960 caagtgtttc ttctgtttga agtgtcttct gtcaccagta agacatgtgt ggcatctgtg 46020 cctggtcctc cttagcctat aacactaaga ctccaaccct gcctagagca tgatgaccta 46080 aattattttg gttgcccaac agccttctgg atgtttcaag agtgtcttca agccaagctg 46140 aactcttacc ttaccatgct cttcctcctc tcttcacagt ttagttagtg gcatcaccat 46200 gtctatgcaa acatcccaca ccagaaactc tggaggcatc tttgactctt cccctgttcc 46260 ctaatcccat acattcagct agggtccatg ccaatcttga ctcagttccc attctgcccc 46320 ctggcttcaa atatccatct ccaggccttt ctgtaacctg tgttttctga ggagtatagg 46380 gtttttaaca ccctttgagg ctggaggtcc ttgagctcct aaagtccaaa cttgggattc 46440 cttgtgagtt tctgaaataa acagaaactc aacatttcca taattactta attctctggg 46500 gagtttgaca tttatagtgg ttaagagttt gggctggagg gcatagctgc ccaggtatga 46560 atctggctct gctacttgct agtttcatga cgttgggcaa gatacctaat ctgtctatgc 46620 ctcagtttcc tcattagtga aatggggata atgatagtac ttacctcaaa gggatttagt 46680 tggaattaaa tgagttaata cagttaaatt gtttagaact tgcctggcaa atagtaagtg 46740 ctcaataaat gctgttgtta ttattactgt cattattaat acctacatta tcttagtagc 46800 tctcgaaggc actgctatat tatactaaga aggctattgt ataattttgc agttttagtg 46860 gacagggaca gttagtaaaa gggcaagtta agttacacag actacataag tccagaagca 46920 tcactatatt actgcatagt acagtaattg ttcataacag tgtcccttgt tttcttttta 46980 ttaataccag atttcaatca aattaaggtc atgaaagttt aattacttat gcactaaaac 47040 ttaccagaaa atataaaata tctcattttc tggaatagat aaacgaagct taattgtatc 47100 aatgagctac cagaatcatt tcattaagga ggtcaccaga ttgttgtagt tagcaaagga 47160 ctctctccca attaggaaat tagtttttct attgagacct aataactgca gaaattagag 47220 catttgtaac aacttttttt ttcgttttct taaatatatc acattcaatc cacctgttct 47280 tttaaattaa gaactgagga cttgtgtaaa aaataaactt tagttccata ttaaaaccag 47340 ttatgatcag gaggaagaaa gggagaggta tgagaataga gaatagaagc aggatacttt 47400 gatgtgtatc agtcactatg tatctggtgc ttaacagctt acactggttt gtttgttttt 47460 cattttgtac ggggctttta cacatacatt atgtagttcc ttagaatagt cttgtggtaa 47520 ggcaattatc atctaaccca ttttatagat gaaatggagg cttacaaaag gcaatttctc 47580 caaactcact gagctaagga tgtggctgag cttgaactca aacccaggtc ttccctctct 47640 ttgaagaaag aaatggggag aaaggaactg gaagagaaaa taccggtcat ttttgaggtg 47700 ctggcagtat cattttactt tcattctaca ctctcatcac atcttctttc aaatgttgat 47760 cagctaattg tttatgtgac acctttactg taccatccta gagagtccat gtgaatgggt 47820 atttaatgcc atgggaaata atttgctgag ctacagaggt agtgactaag gcagtgtcac 47880 cccaggagct ctctactctt aatctagact gcagaagatt ttctttcttc tcctgactcc 47940 cattttaaaa ctctggcaga aaataattag cctaaatgag ctccttggtg gaatcattgc 48000 acttggcatt gttagaaatg caaagagtat tattcacttg attatctaat ctatttatat 48060 ctaaaagttt ctccagtatt tacgtttgtc cgttagtttc caaaatctgc ctaattccca 48120 acagactcca cataaagaca tggtataaca ggatatatcc atggtctctc attcctttct 48180 gtcaagatat gaatggtctt taaaggcccc acttgctgca atgaaccaga aatatcttca 48240 aatctttaac aaaagaccta cattttatga ctttgtaaat tcatttaaat ttgtttcagc 48300 aggagtgaat aatttattat agctgtaaaa ggaaggaaat atgtagtcgc ttttcttaac 48360 taaagtaatt cagattttca aagaatagcc ctatttgtaa agaaattatg catgtgggat 48420 agggatggtt ttgtctctgt aagtaaagca ttttttttaa aaaaatcaaa actactaaaa 48480 ccttaagaca caaaataaag gatgaattta tagtgtcttt ggtacctata gtatgtgtgg 48540 cagattcatg ttgatgtctg gggattccaa tttttatatt tttattgtat tagaaaaatg 48600 tttttttctt acacttggaa ggaaataatg agatgtgaag gaaattttca tgcgtatata 48660 aaatgtattt agattattaa aataattaaa tttaagtgtg aaaagatagg ggaatgtcta 48720 cttaggtaaa tatttttagt tcaaatattt ttagtacatg gtattcaaga aacatgttta 48780 gttgttctac agaattttaa acttcaaccc taacatctgt acttacttct actagtgctt 48840 ttactatcac ccaatgactt ttagnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 48900 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 48960 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49020 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49080 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49200 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49260 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49320 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49380 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 49440 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnaggtt gggaaaatat 49500 ttcaagtggg atccaaaatc attgttttaa tattgtattt catgtagcat tgcagatgaa 49560 agaggaatat gtaacttaag aatttatttc attttttaga aaaaatacta tatataattg 49620 tggtaaatag tacaaccact aaaaaagata atcaaataaa cgccaatgaa attttcatct 49680 acattaaaag ctgaagtttc tagatgtggg ttgcttgatt atatcttaga gctcaggact 49740 agaatgatgt aatattttat ttttctatta cagatgactt gtttaaagtt cacaagctta 49800 agccaaatct gaagtggcga caggcttttg acagctactt aaaaactctg cctccatact 49860 acctattagt atgtatttgt gtgtatatat gtattaactg tatcaatgat aattcttgtc 49920 acaagaaatg ttagtgatca aaagctttta ctgttgcaat aagagagata tctttttatt 49980 ttacagatat ttgtgtcgtc actgtcttct caaatcatgt gtaagagttt ggagatgtca 50040 tggcggcaca aaagagagct gttttctcta ttttattcct ttaactgcca tggttatttt 50100 tataaaacac atctatgttt ctcttattaa aagtaacctt aatttcattg ggaatttaag 50160 aataaataga tctggattca tatattacat caacttccct ttttaactct agaaattctc 50220 agtatggggt ttccctctgg aaaaagaaaa tctgaagaca ttacagttgc ctattgcctc 50280 ttaaatgtgt cctagacaca gcatgaagtt ggggcactgg tggtgagagg cggaatccaa 50340 aaaaattcag aaatgacttg gcctcatttt ggatttcata atgtgaagta ttcatgattt 50400 tgaactggta atataatcta aatcaagatt accaaaataa tttcagaggt tgatgtggta 50460 acctttaagc gaagtttcta gaggtgaaaa ggcagaatct taaatggtac cattggtgtc 50520 actgggagga gaaattgggg tgtgttactg tttaccatgg cagtaatggg gcaaacaata 50580 aaatgcaatg tgaaatgatt tgatgatttg ggaaataaga ttgaacgcaa tttacttgtt 50640 tgaatttgct gttacttgct cttcttatcc cactctcttc tgattttttt ttactttctg 50700 ctccttactt ctctgctatt ttcattgcca ctttttaatg ttccatgttt ggttttatgt 50760 gcagcacctt gacttctaag aaatgaatca tgtccctttg ccccttataa ctgaactttg 50820 agtattttaa gatttattct attcttactg ttgtgtattt tgtttcctta tagccattaa 50880 agaaagcact aaggatgatg ggagctccaa atctgatatc agataattta gattgtggac 50940 ttagttacag tgttatctct taccttaaaa aactcagcca acaggtagta ttggtaaaaa 51000 caaacaaaca aaaatccttt gccctcagaa gtgcatttcc ttattcttta gtgtaattgt 51060 aatttttcaa attaaatgtg tatatatctc tacactttat ggattagtaa taatgtgatt 51120 ctctatggct tctagcttca ccattaagct gcagttaagg gtctgtcagt atcatttgat 51180 gctgtgccat ttctcctttt gcctgccagt ttgtcctacc cgcaagctgg ttgatatggg 51240 gcagaggttt aatagacttc tctcatgggt cacattttgt ctatcttcaa cctagttcct 51300 cctcagatca ctctgggcta cagcatccct cctgtttaga tcagcacact gaggcgtggt 51360 gtgattaaat gacttgtctg agattagttt tcaggcatgt gaaggactta tactcacatg 51420 ctagcccttg gataaagagc tatatgcttt tccctggaga gtggggagat gagaccagtg 51480 ttcctcacac tggagggtga tagaccccaa ggggaactga agagtggagc tcagtttcct 51540 ctcttctcac cctccacctg ttcctcattt gccattattc accttgtccc ttgcctgccc 51600 ctctctatta gtacctcatc ctccactcac cgttccttat catacttctc acctctactt 51660 agcccattct tgtaggatgg aaatatttga gaactactga gttagaactt tactatcata 51720 tgaatgtgtt atgttatatg acaaattaat gcagcagttt tacttacctt atgcacaaag 51780 gtattcccag gtaggggaca atagtagcat tcgcagtggt gataatgctt caaggtggat 51840 gtgtttggaa gtttggcctt taggaaatgg agagtagtga gcaaaacatc agatttcacc 51900 aaagaaccaa agtgactcca caattgggat gccgacacac cttgctagga actgacaaca 51960 acttcagtat ggtctggagc ttaccagctc ctaccagtcc agtgtgctta taagtgcaaa 52020 agaaagtaaa ggcaacccca gatttctaat ctaccaagtg tccccctaac ctcctttcct 52080 ctctgctaat agattttttg tggttgttgt aaatgttttg gtttggttat ttatttattt 52140 atctatctat tgatctatcg atttttttta atttgatgtt tacctaagcc tttaaggctg 52200 tgtcaccaag gtatggccac aaggaagaat agtgtacaga gattttaatt aatgcaagtt 52260 ctgggacctt ttggggcaca tgtatcattt tacaaatgag ctttcaagac catttaagga 52320 aacagatgct tcatttgctc ttatctcata tttcatgact taagaatttt ttagtgataa 52380 taaacataga cttaattcca ataattaggg aaaattgata aatatctgtc accaaaccac 52440 aagaaatcca aaatcatttt aggtttacca aacattggtg gaattccatc tttctgagaa 52500 aaagggaaga tcatagctaa tttataatag ctcaaattac taatttaata actgggtcac 52560 cagtgtttct tgagccattt cagatgtatg taaaacacaa aatatgccaa atatatattg 52620 ctataataca ctcaagcagt attaatcaat atggtatcac aatgcctatt aagaggcttt 52680 ttacaaatta cttacttagt aatatctgtt aaattaagca ttatcttcta agaccttttt 52740 tggatagtca aatataagag ataaatagtt taattttttc agaccttttt tggatagtcc 52800 aatattagag ataaatagtt taattttttc agatataatg ccagtcgatg tgatctgaat 52860 tttagtacta gtttacacgt ataaatacag tcttaaacct ttatgtctga gtctgaaatg 52920 aacctgttca cttagactag attttatagt aacaaaatgt gcttttaaat gtctatgaat 52980 gaaattctta ttcatggttt ttattctctc catgatttta ttataatttt gacactagac 53040 aagaaaaaaa aatattattt gtctttcctg ccccctatct gtttgctgtg atagtgcaaa 53100 gaagcacagg aaaatgttta attatccatt tttctgtgat ttgtaattga aaattgttct 53160 gtggggttct gaaagtatta tctttcttaa gtagtaaaaa tgacagtggt aatgtagatg 53220 tttttataac atactatgta ctttcatttt agaccaaact agagtcagaa cnnnnnnnnn 53280 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53340 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53400 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53460 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53520 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53580 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53640 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53700 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53760 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53820 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 53880 nnnnnnnnnn nnnnnnagaa agtcttggcc agcacagtgg ggacctctag caccaagatt 53940 tcctacagag gagggccaca ctgggcagag ctggccaggc cctaacaccc tgccattgtc 54000 tgttactggc tatgggcagc ctgggaaggg catggcctca gctcagtgct gcagcggatc 54060 cctatggcac cacagcagcg ggaggctctc tgctaactgc actccttgca ggatcagcca 54120 ttgctttcct gaagggagat cccagcagct cacctcccct ccatggctgc cagaggaata 54180 catctagagt acgagcagtg gtcctgcaag gcggccacag gtatcaatct cgggatttgg 54240 tgttttaaat gacatatttg aaaagggata gtcccagtgg ctttaatacc ctgtaggtgt 54300 gttacaatgc agaacaaggc tagcaagtgg aattttgcca ctgggaaaat tctactgtag 54360 tcagttgtat tgatataaca ctcttcaata acattttaag agagataagt atgacatttc 54420 tatattaaaa gccttaggag taactgaaat tatttgtttc atttcaaata ggatttgaaa 54480 cctcagacat acagaaatgc ttatgatatt ccccgtagag gtcttttaga ccagctgacc 54540 agaatgagat ccaatctgct gaaaacgcac aagtttattg ttggacaaga tgaaggtaaa 54600 ataactgtga aatacttttt tttttttttt ggaaaatgcc aggcatgact tacaggaagg 54660 tgtttattgc ataatgagta ggctatttta tagtatttta atgtttaaaa tgcctgtttt 54720 cactgaatcc ctatgtctgt ttaccaggca catttttttt ttcaagttta aggtcaagtg 54780 tgcattaatc agcacgtaca ctacacttgc catgctttag ctattgtaag cttcaaacaa 54840 ccccaggaaa tagatactgt ttttatgtcc aattcatgga catggaaact gagagtgagg 54900 atttttagta gtttgcccaa gtttagccag ttggaaagtg gcagaaccta ggtctgtcag 54960 atttcccaat ttgcacaccc aaacactaac actcagccta ctgtgataaa ttcagtagag 55020 aatacctcat ttaaatgaaa gtaatcaacc taatggtatc caggataatt gtgactattt 55080 acaaattcca tttactccat tttgttaatt ttaaaaaggc tcacctgttc actaaaatga 55140 gcaaatctta ttctggtcaa ttccctgaaa ttatacacaa agttttgtgt gtaagagggc 55200 ttttctagga agagaaccta cagatttaat caaattctca ggattaagac ctactaacca 55260 agattctctg gatgataagt gaatgccata gagactagac tctttgaaat gcagaagata 55320 tgtggtgatt tgagttggga tggtggtgta gggtcagccc attctcaaac ctggtttgaa 55380 ggcaagggag ttgttctgat cctagcgatg tgagcctgta ggcagtagta acggtagact 55440 aagttatgat tgggatgaag agagatgatt ctagatccta gaatgctaga ttcgagactt 55500 taaatactat ttgatgccaa gacacacact gctaaaccaa actatgatca tgtcttctcg 55560 aaaggaccat acgcttcagc tataagcatc aatttctttt cctgtgattt tgcagattcc 55620 cttcatagtg ttccagttgc acaaatgggt aactatcagg aatatctgaa gacattggct 55680 tctccactgc gagagattga tccagaccaa cccaaaagac tgcatacttt tggcaatccg 55740 tttaaacaag ataagaaggt aggataccta tgcctatgtc tgcctaaatt gggatattct 55800 tgctatataa ttattttctt tttggcaaga taaatacaaa tcagaggttc ttcatttgtt 55860 tgtttaaaca ataaaatatg acactaaggc tcttagtggg agcctcctga tgcaagagtg 55920 tgttggttga ataaagtcag agctgccatg tattgagtac tagtaggagc tggtgtttta 55980 aatgatctca cttaatgctc acaactgttc tgtaagacaa atgttactgt ttgtccttta 56040 aaagggagaa atcaaaggcc acagtggtca aacgccttac ctgtgacata gcacataaga 56100 gcaaggattt gaatccacgt ctttctcact ccagaatcta tattcattcc accacacact 56160 aatttcttta atatcaaaat cacagtttat ttcctgtttc catgattcat atctgtagtg 56220 cttgatctag aaaacgatga atgtgtccct tgaaatatga agtactaagt gatgttgttt 56280 tacttgaatg gtcctactaa aaatctaaat gtggggagtg tgtgtgtgtg tgtgtgtgtg 56340 tgtatgtgtg tgtgtgtgtg ttatactgac ttgcccatta aagcatgaaa acaaatggga 56400 ttatagctgc actcatggag gagaccattg gtgttaatta aggctcagac cacacaataa 56460 tctcttttgt gacaagactg attgaaaggt attccacgtc acctaaatcc tcaatttatc 56520 tttctatgct tcactttcct cattttgtag cactgggaat aataattaca cctaactatg 56580 ctggacgagg tggctcacgc ctgtaatccc agcacattgg gaggccgagg caggcaaatc 56640 acttgaggtt gggagtttga gaccagcctg gccaacatgg caaaaccctg tctctactaa 56700 aaatacaaaa attagccagg cgtggtggtg ggtgcctgta atcccagcta ctctggaagt 56760 cttaggcagg agaatcactt gaacctggga ggcggagatt gcagtgaacc aagatcgtac 56820 cactgcgctc cagcctgggt gacagagtga gactccatct caaaaaaaaa aaaaaaaaaa 56880 attacaccta attaactaat agaactctgc ataatattaa gtgagtacat gtacattgtt 56940 tacaacatga acaggcatgt agtaaattat ctgaaaatgt tttccccttt ctgtattgtt 57000 tatgagtaaa aaatcttttg gaaaagccat ttattattat tttattcaac taatgagggc 57060 acatattctt ggattattcc tggacaagaa cagctcttgg ctaaatttct atactgctgc 57120 ctctcatctt ttatctatcc ccccaagagt gaaaagcctc ctcactgcct gcccagcacc 57180 aaagtgggca tatttgaatc tctgtgaggc tgcagatggg gaagttacat tttccacctg 57240 cctgcctttc aacacgtaca tgtagcatac tgtacagtga taatcaatgt tgtttaatga 57300 tatgagtttg gagcataaaa aaggaaatta tttcccttat gaagagttga tgcaaaatag 57360 ttcgtacttc tctccttttg gttgaataat gctgcttatt tgcaaacttt ctgattaatc 57420 attattgtag tatgttttgc ttgggacaac atcctgtatg ttagtttcct ccttgttcca 57480 tttaaattgg attaaaattg agttgcatat ttctaagaac aaagttgggg tggggtaaga 57540 taaatcttcg gcccatgatt aaggtttata ttagttaatc tggcatggga tttaaaaaaa 57600 tgaaagaaaa aaagacatat tcgtgatata atgcaagatt gattatgtat gcatattaag 57660 agtgcttgca gttatataat agtggaattt tggtctttaa tgaaatacgt tcatttatgt 57720 gttttttagg gaatgatgat tgatgaagca gatgagtttg tagcagggcc acaaaacaaa 57780 gtgaaacgtc caggggaacc caacagtcct atgtcatcta agagaaggcg gagtatgtcc 57840 ctgctgttga ggaaaccaca aacaccacct actgtaacta accatgtggg cggaaaggga 57900 ccaccctcag cctcgtggtt cccatcttat ccaaacctca taaaacccac ccttgtacat 57960 acaggtatag agtagtggtt gtgatttcct tatggctcct agaggactaa gacgctaaac 58020 aattttattt ccctttttgt gttccttcct ttgtgttcag tttgtgttca ttaagtaagc 58080 cattactaaa tcatctattt ggtaggtaca ataaacccca cagggagcag agaccctgtt 58140 tcaaggatct caatctacat gaggtgaaaa aaattataat tatatagtaa ttaacacaca 58200 gtaattaaca gtaatgaata cattgcttag caagtaaatg ccacagtaat taatggagaa 58260 atggaaagag gtgagcatgt ctgctgcaac cttttggagt ggctgcaagg gtgaggagga 58320 taaagcaggt ttccctggca gtaggagcaa gtggactcag caagactgga tctgcacttg 58380 ctctttgtgt tatcaccacc tatgcatgct ctaatccggt gcagtctggt atctgcctcc 58440 tcgaccccac tgaaacattc tcatcaaggt cactagtgtg tgcagcacat tgccattcct 58500 tctccacagc atttgacaca gttgttcact ccctcctcca tgtgtacgtt gggtgctcag 58560 acaccataag cttatagctt tcttttccct ctaatagcaa ctccctttca acctcttttt 58620 ctggttttgc cttttctttc cacctctaaa tatcataggg cctcaaaact caatcctggt 58680 acctctcctg tccttcactg cgttctcttc ctaggtgacc ccatgcagtc ttggggctct 58740 aaatttgacc tctagaatat aaattgctcc tcaatttcag actcagactt acttgtggac 58800 atgcatctcc acttaggtgt ctaatagaca aataaaactc agtaggtttc atgagtttca 58860 actgaactct cgaacttgcc cctctccaaa acagctctac ttgtagcctt ccacattgca 58920 gataatgaca ccatccagat atgtgccagt aaagctttaa catctgtcag ggttgaggag 58980 ggtagagaag ctctagattg tagtgtttgc agatttcctt catgtaaata atgctaatat 59040 ttatcaaagt caagctgtca acctgaggtc attgaaccag agtcgggaag aatgctctgg 59100 agggcagttg tgccctggct cctgccacac ttcagcacta tttacccagc ggctcagctg 59160 acaaaccata gagtcatcat gatttttctc ttattcttcc ctcgctttga tacctttcac 59220 aagttcagga aacttgatgt tcaacataat ccctaaatcc cactatttct ctctatccct 59280 ccagtgcaca ctgctgtggc ctctcaccac actactacaa taccttctta tcccagcttc 59340 atgtttctaa tctagccccc atctatcaca tactctctaa ccctgtggcc agaaaattat 59400 gtctgcatgt atatcacatc atgccatgtc gctcctgaaa acctgtcctc aactctcctg 59460 agcactcaga agggaccctg aaccagcttt agtctgcaag actgcacggc tggcctctgt 59520 caccttctcc taacacggga gcccctgggg ctccctctgc tgctgtctcc caaaggcctg 59580 tagatgactt ccccaacacc agcccaatgc tgcttgtttc atttgctcat tgtgcatgta 59640 ctgtctgact gccccatgag gatgtgagct ccacaagggc agggaacgtt gctctggctg 59700 tttactgctg atctccagct cccgacacac tgcctgccac agacgatgaa taaatgaaag 59760 aggtgtcaga tctggagtga aaagaaagta cttttctgac acagaaaaga aggattagga 59820 agataataca ctaagaggga tttttggtga tggagtgtgt atagaacttt cagcactaat 59880 ggccgcctct attttctcag aatgtatttg atgtaaagag gaggcaggtt gtggtgtatc 59940 caagttgtct ggcttccagc tcagtaaagc atggcaggtt gtatgtgaat ttgagaaatc 60000 atgaaataaa gtgagacttg ctgttttcaa cttgaaaagc ataacaagct gacactaacg 60060 catgagtacc agggatctgt gaatgtgtgt ttagagttgt actgtcttac ttggtttcca 60120 tatgtattca tagggccaga aaataagagg tggttttatt gtattatgtg tcctggcctc 60180 aatttgaggg gtctcagatc gccacctggt atatcatcct gctttatgag ataatttcct 60240 agaaattgag catcagaggg atatacctgt ggggttgaca taataccctt acctcacagc 60300 tcaacctctt catttggttt ccagatgcta ctatcattca cgatggccat gaggagaaga 60360 tggaaaatgg tcagatcaca cctgatggct tcctgtcaaa atctgctcca tcagagctta 60420 taaatatgac aggagatgct tatgccaccc aaccaagtgg attctctatc ctgacgactt 60480 cacaagtact cagcaaagat gggctgattc aaaaacctgg tagtaacgca tttgtaggag 60540 gagccaaaaa ctgcagtctc tccgtagatg accaaaaaga cccagtagca tctactttgg 60600 gagctatgcc aaatacatta caaatcactc ctgctatggc acaaggaatc aatgctgata 60660 taaaacatca attaatgaag gaagttcgaa agtttggtcg aagtaagtag tgaaagaaca 60720 tctatcaata atgcaccagg aggtttctct cattctgtga ttcactatag attcaagcta 60780 tcccttgagg tacactgggg gcaatattgg gctttcacat agtttaaggc agttcctctt 60840 gttttaacta aaaaggtaca gtctatattt tcctgttttt tccccttatt tcttgtaatg 60900 tttccttttg ctgccgtaac aagttatcaa aagattccta gcttaaaaca atacaaatta 60960 ttatattaag ttctggaagt cagaattttg aaattatttt tgctgggcca aaatagtgtt 61020 ggcagaccag cattccttct gctagctcta gagagaattt ctttctttgc cttttcgagc 61080 ttctaagggc catctgtatt ccttggccca tggccccttc ctccatcttc atgaaaacac 61140 ccttagcact ttttctcctc tctgacctct gcttctgtct ttacatgttt tctctctgac 61200 cttaactcta ctgtttcatc ttataaggac acttgtgctt acattgggcc cacatgcata 61260 aacttggata atctccccat ctcaagatcc ttaacttaat tacacctgca aagtaaagtc 61320 ttttttgcta tataaggtaa tgtattcaca ggttccaggg attaatatgt agacaatttt 61380 aagcagctgc tattcagcct gctacatttg gttagtgtta acaagagttg ccctagtaga 61440 tgcatgcaga tattttgata agaatgttaa aatacaaact acatctaact ttccactcac 61500 gaagaacaat tactaaggat gtacaacaat taaattttat ttcccattca tctttataaa 61560 aatactgaag tttttttaaa tatcttcaga atatgaaaga attttcattt tgcttgaaga 61620 agtgcaagga cctctggaga tgaagaaaca gtttgttgaa tttaccatca aggaagccgc 61680 aaggtaggta taaacaggaa ctcttcaatt ttttgttttt gtttttagag cagtagggcc 61740 cagtgcagga aaaagagagg aataggctct gccttgcttt tttctcaaac cctggccctc 61800 actcatagtt aaggctgtct ccagaagtat ttggatttat gttatctgaa ctcaactcat 61860 tcatccttct acttttatca tagcctcagg taggcttggg ccctcaattg ccactattgg 61920 tacttgctct aagacatatc tttccatgag gacaatcttt atattcctat gtagattgta 61980 agcttcgatt tgtatcccac acagtgcctt gaacatcatg agtactttaa gtatcttttg 62040 gttcataaaa tttctcttta ttttcaggtt taaaagacga gtcctaattc agtaccttga 62100 gaaggtacta gaaaaaataa attcccacca ccttcacaac aacattagtc acatcaacag 62160 cagatcatca tgttagtgca aagaccagtg agaaaaaaat gacaagtttt ctgtgctgta 62220 ggatggaaca ggatattgtt gaagcctcct ggaatgtttg agtcaaggga attgctttcc 62280 agatgctaag aagcagcagt ggggcttttt gaattttatg attatctggc agtgaaagct 62340 gggcttttgc cttaataatt ttttaaagta tgaattgttt tgttttgttt tcctcaattg 62400 aggaagctga tgttattaat tcacaggcta aattcggtaa acaccactgc ccctaccacg 62460 ggtaatgaga ggtcactcac ttgaactttg ccattccagg cattctcaga gtggcgaggg 62520 gccacctgca agtggagcac aacttggtgc tcttactgtg tccttcagaa agaataggtg 62580 tacagaaagg aaatggcaat cttatgtgtg ctgaacaaag ttttcaacaa ttcctagttg 62640 tgccttttaa accatgcaat attcaggata gtttgaatca aagaagtaag aagctgctat 62700 ttgggtaact tatttctctg tgggaagggg cagggagagt caccaaacaa tctacctcca 62760 actctcttct cttttgtcta gagacattac aaagtgcact tgaggctgcc cccaacctct 62820 gacatttgtt cttgcatgtg atgatagaaa gtcttcagat ggacttatac attctgtgct 62880 ttggaagcac aagaagaaca aaatatgtgt atatttcctt taatgtttat acaaaagttt 62940 atatggagca gtattgttat gtttgtatga atttgcaaaa attaaagtgt acaaagagat 63000 tttgattttg catatataaa ataaatcatt ttattgattt tcacaagttc attaatgctg 63060 gataaatttc tacttatatg tttcttgtga tttgttactc ctttcagaaa aagagtgtat 63120 gctgttaaac aagttaagat gttaacataa ggatttaaac ttcaaaacat cactcacaga 63180 attgagtgac gctagtgaaa aatcacagag tagagtaccc acggactagt cactttcaag 63240 aaacttggaa aacactgggg gaaaaaaaaa cctgtcagaa tcaagtttta ttggaactct 63300 agaatatagt aaaaggttta cagcaaccaa gccaatcctg aattaggaga gaagtcattg 63360 aaacatggta ggggagcttt gtggcatttc aactcaccct tggaatggct gagtaagaaa 63420 gaaatttgag gccaggtgca gtggcccaca tctgtaatcc cagcactttg ggaggccaag 63480 gtgggaagac cacttgagcc caggagttca agagcagctt gggcaacatg gcgagacccc 63540 atctctccaa aatatatgta tttttaatta gctggacgtg gttgcacaca attgtggtcc 63600 cagctactca ggagactcag gtgggaggac tgctggagcc caggaggtgg aggctgcagt 63660 gaactgtgat cacaccactg aactccagcc tgagcaacag agcaagaccc tgtctcaaat 63720 aataatatat acaagctgac ttctgaaatg gcatggctgc ttacttccca ccttcctacc 63780 cctctcaaac aaagagggag tttttgcatt ttctattcct ggttgcaaaa cacaaaggaa 63840 aatggaaaaa tagtttgtgt gcattcatga tatgcttgct cctttgagac tctcaaacag 63900 ccagcaccat cccttcccat agcctgctag gagccaagat ggcttcccag tgcctgtttc 63960 tcgaccattt taatttaaaa gcatggtgag tagtattagc tgtgccttct ctgccacagg 64020 agagaaagcc tggtcaagag gtgtggtttt ggatgcaata agtccactgc ttcttggaga 64080 cgttcctgga cattcaatcg tgtctttcct gggtccttgg agtagttggt caggatgggc 64140 ttcccactca gtccacgggc ctggggctga ttcatggtgg tcccagagac ctcagccctc 64200 tgtgtttggc tggaagccca gaatggtgta cagttcctca ggcatgagcc ccagcaagtt 64260 ctggacgtca cacaaaaagc agcacatata gcactttccc gacatcttat ggatgatgtt 64320 cttgtcatga tagtaggtaa acccaggctc agcttcttgt agttcatctt gggcttattt 64380 ttcctgattc cccactggca ggcaacattg tcagggttgg caagtttaaa ctcccacctg 64440 tccctattcc agctgatgaa atgactggca agactgtcta aaattccagg aaaaactgct 64500 gtgggtgaat aggtccactt tctgtgaagc cagacagcac agccacaggt ataactggtt 64560 tgccttgctc caccgggttg ctcctctctt ggatgtaatc cttgaaaggc atggtcaact 64620 ttttgaggca gggggactga ctgcagtttt ctttgaagct ctcgaagaaa ggaacctgct 64680 gcacatccag taaggatgac tggttgttcc aggtgcctga gctctcaaag ctgtctgcct 64740 catgatttaa atgttaaaaa agcagacagc tttaaatgtc tgcaccattc tcaggggatt 64800 tgtggtcttt aggcttccca gaattgttgg tgagcaaatt caagttgcct agaaagtcct 64860 gactgatgga gcatagttga ggctgataga gctgagctga gacttggaga acatctgaaa 64920 ctcctgttca gagctgagca cgctgggtgc agaagctgga cacatgctgt ccaggaggct 64980 gcctttgggg taattgtgtg tttgcatacc atagggtacc tgctttatgc caaaacctaa 65040 tg 65042 4 886 PRT Human 4 Met Pro Ile Leu Leu Phe Leu Ile Asp Thr Ser Ala Ser Met Asn Gln 1 5 10 15 Arg Ser His Leu Gly Thr Thr Tyr Leu Asp Thr Ala Lys Gly Ala Val 20 25 30 Glu Thr Phe Met Lys Leu Arg Ala Arg Asp Pro Ala Ser Arg Gly Asp 35 40 45 Arg Tyr Met Leu Val Thr Phe Glu Glu Pro Pro Tyr Ala Ile Lys Ala 50 55 60 Gly Trp Lys Glu Asn His Ala Thr Phe Met Asn Glu Leu Lys Asn Leu 65 70 75 80 Gln Ala Glu Gly Leu Thr Thr Leu Gly Gln Ser Leu Arg Thr Ala Phe 85 90 95 Asp Leu Leu Asn Leu Asn Arg Leu Val Thr Gly Ile Asp Asn Tyr Gly 100 105 110 Gln Gly Arg Asn Pro Phe Phe Leu Glu Pro Ala Ile Ile Ile Thr Ile 115 120 125 Thr Asp Gly Ser Lys Leu Thr Thr Thr Ser Gly Val Gln Asp Glu Leu 130 135 140 His Leu Pro Leu Asn Ser Pro Leu Pro Gly Ser Glu Leu Thr Lys Glu 145 150 155 160 Pro Phe Arg Trp Asp Gln Arg Leu Phe Ala Leu Val Leu Arg Leu Pro 165 170 175 Gly Thr Met Ser Val Glu Ser Glu Gln Leu Thr Gly Val Pro Leu Asp 180 185 190 Asp Ser Ala Ile Thr Pro Met Cys Glu Val Thr Gly Gly Arg Ser Tyr 195 200 205 Ser Val Cys Ser Pro Arg Met Leu Asn Gln Cys Leu Glu Ser Leu Val 210 215 220 Gln Lys Val Gln Ser Gly Val Val Ile Asn Phe Glu Lys Ala Gly Pro 225 230 235 240 Asp Pro Ser Pro Val Glu Asp Gly Gln Pro Asp Ile Ser Arg Pro Phe 245 250 255 Gly Ser Gln Pro Trp His Ser Cys His Lys Leu Ile Tyr Val Arg Pro 260 265 270 Asn Pro Lys Thr Gly Val Pro Ile Gly His Trp Pro Val Pro Glu Ser 275 280 285 Phe Trp Pro Asp Gln Asn Ser Pro Thr Leu Pro Pro Arg Thr Ser His 290 295 300 Pro Val Val Lys Phe Ser Cys Thr Asp Cys Glu Pro Met Val Ile Asp 305 310 315 320 Lys Leu Pro Phe Asp Lys Tyr Glu Leu Glu Pro Ser Pro Leu Thr Gln 325 330 335 Phe Ile Leu Glu Arg Lys Ser Pro Gln Thr Cys Trp Gln Val Tyr Val 340 345 350 Ser Asn Ser Ala Lys Tyr Ser Glu Leu Gly His Pro Phe Gly Tyr Leu 355 360 365 Lys Ala Ser Thr Ala Leu Asn Cys Val Asn Leu Phe Val Met Pro Tyr 370 375 380 Asn Tyr Pro Val Leu Leu Pro Leu Leu Asp Asp Leu Phe Lys Val His 385 390 395 400 Lys Ala Lys Pro Thr Leu Lys Trp Arg Gln Ser Phe Glu Ser Tyr Leu 405 410 415 Lys Thr Met Pro Pro Tyr Tyr Leu Gly Pro Leu Lys Lys Ala Val Arg 420 425 430 Met Met Gly Ala Pro Asn Leu Ile Ala Asp Ser Met Glu Tyr Gly Leu 435 440 445 Ser Tyr Ser Val Ile Ser Tyr Leu Lys Lys Leu Ser Gln Gln Ala Lys 450 455 460 Ile Glu Ser Asp Arg Val Ile Gly Ser Val Gly Lys Lys Val Val Gln 465 470 475 480 Glu Thr Gly Ile Lys Val Arg Ser Arg Ser His Gly Leu Ser Met Ala 485 490 495 Tyr Arg Lys Asp Phe Gln Gln Leu Leu Gln Gly Ile Ser Glu Asp Val 500 505 510 Pro His Arg Leu Leu Asp Leu Asn Met Lys Glu Tyr Thr Gly Phe Gln 515 520 525 Val Ala Leu Leu Asn Lys Asp Leu Lys Pro Gln Thr Phe Arg Asn Ala 530 535 540 Tyr Asp Ile Pro Arg Arg Asn Leu Leu Asp His Leu Thr Arg Met Arg 545 550 555 560 Ser Asn Leu Leu Lys Ser Thr Arg Arg Phe Leu Lys Gly Gln Asp Glu 565 570 575 Asp Gln Val His Ser Val Pro Ile Ala Gln Met Gly Asn Tyr Gln Glu 580 585 590 Tyr Leu Lys Gln Val Pro Ser Pro Leu Arg Glu Leu Asp Pro Asp Gln 595 600 605 Pro Arg Arg Leu His Thr Phe Gly Asn Pro Phe Lys Leu Asp Lys Lys 610 615 620 Gly Met Met Ile Asp Glu Ala Asp Glu Phe Val Ala Gly Pro Gln Asn 625 630 635 640 Lys His Lys Arg Pro Gly Glu Pro Asn Met Gln Gly Ile Pro Lys Arg 645 650 655 Arg Arg Cys Met Ser Pro Leu Leu Arg Gly Arg Gln Gln Asn Pro Val 660 665 670 Val Asn Asn His Ile Gly Gly Lys Gly Pro Pro Ala Pro Thr Thr Gln 675 680 685 Ala Gln Pro Asp Leu Ile Lys Pro Leu Pro Leu His Lys Ile Ser Glu 690 695 700 Thr Thr Asn Asp Ser Ile Ile His Asp Val Val Glu Asn His Val Ala 705 710 715 720 Asp Gln Leu Ser Ser Asp Ile Thr Pro Asn Ala Met Asp Thr Glu Phe 725 730 735 Ser Ala Ser Ser Pro Ala Ser Leu Leu Glu Arg Pro Thr Asn His Met 740 745 750 Glu Ala Leu Gly His Asp His Leu Gly Thr Asn Asp Leu Thr Val Gly 755 760 765 Gly Phe Leu Glu Asn His Glu Glu Pro Arg Asp Lys Glu Gln Cys Ala 770 775 780 Glu Glu Asn Ile Pro Ala Ser Ser Leu Asn Lys Gly Lys Lys Leu Met 785 790 795 800 His Cys Arg Ser His Glu Glu Val Asn Thr Glu Leu Lys Ala Gln Ile 805 810 815 Met Lys Glu Ile Arg Lys Pro Gly Arg Lys Tyr Glu Arg Ile Phe Thr 820 825 830 Leu Leu Lys His Val Gln Gly Ser Leu Gln Thr Arg Leu Ile Phe Leu 835 840 845 Gln Asn Val Ile Lys Glu Ala Ser Arg Phe Lys Lys Arg Met Leu Ile 850 855 860 Glu Gln Leu Glu Asn Phe Leu Asp Glu Ile His Arg Arg Ala Asn Gln 865 870 875 880 Ile Asn His Ile Asn Ser 885 5 770 PRT Mus musculus 5 Gly Lys Lys Pro Leu Phe Leu Gly Lys Pro Ala Ile Ile Ile Thr Ile 1 5 10 15 Thr Asp Gly Ser Lys Leu Thr Thr Thr Ser Gly Val Gln Asp Glu Leu 20 25 30 His Leu Pro Leu Asn Ser Pro Leu Ala Gly Ser Glu Leu Thr Lys Glu 35 40 45 Pro Phe Val Gly Ile Arg Asp Tyr Leu Leu Leu Val Leu Arg Leu Pro 50 55 60 Gly Thr Met Ser Val Glu Ser Glu Gln Leu Thr Gly Val Pro Leu Asp 65 70 75 80 Asp Ser Ala Ile Thr Pro Met Cys Glu Val Thr Gly Gly Arg Ser Tyr 85 90 95 Ser Val Cys Ser Pro Arg Met Leu Asn Gln Cys Leu Glu Ser Leu Val 100 105 110 Gln Lys Val Gln Ser Gly Val Val Ile Asn Phe Glu Lys Ala Gly Pro 115 120 125 Asp Pro Pro Pro Ala Glu Ala Glu Gly Gln Pro Asp Ile Ser Arg Pro 130 135 140 Phe Gly Ser Gln Pro Trp His Ser Cys His Lys Leu Ile Tyr Val Arg 145 150 155 160 Pro Asn Pro Lys Thr Gly Val Pro Ile Gly His Trp Pro Val Pro Glu 165 170 175 Ser Phe Trp Pro Asp Gln Asn Ser Pro Thr Leu Pro Pro Arg Thr Ser 180 185 190 His Pro Val Val Lys Phe Ser Cys Thr Asp Cys Glu Pro Met Val Ile 195 200 205 Asp Lys Leu Pro Phe Asp Lys Tyr Glu Leu Glu Pro Ser Pro Leu Thr 210 215 220 Gln Tyr Ser Arg Arg Lys Ser Pro Gln Thr Cys Trp Gln Val Tyr Val 225 230 235 240 Ser Asn Ser Ala Lys Tyr Asn Glu Leu Gly His Pro Phe Gly Tyr Leu 245 250 255 Lys Ala Ser Thr Ala Leu Thr Cys Val Asn Leu Phe Val Met Pro Tyr 260 265 270 Asn Tyr Pro Val Leu Leu Pro Leu Leu Asp Asp Leu Phe Lys Val His 275 280 285 Lys Ala Lys Pro Thr Leu Lys Trp Arg Gln Ser Phe Glu Ser Tyr Leu 290 295 300 Lys Thr Met Pro Pro Tyr Tyr Leu Gly Pro Leu Lys Lys Ala Val Arg 305 310 315 320 Met Met Gly Ala Pro Asn Leu Ile Ala Asp Ser Met Glu Tyr Gly Leu 325 330 335 Ser Tyr Ser Val Ile Ser Tyr Leu Lys Lys Leu Ser Gln Gln Ala Lys 340 345 350 Ile Glu Ser Asp Arg Val Ile Gly Ser Val Gly Lys Lys Val Val Gln 355 360 365 Glu Thr Gly Ile Lys Val Arg Ser Arg Ser His Gly Leu Ser Met Ala 370 375 380 His Arg Lys Gly Phe Gln Val Leu Gln Gly Ile Ser Glu Asp Val Pro 385 390 395 400 His Arg Leu Leu Asp Leu Asn Met Lys Glu Tyr Thr Gly Phe Gln Val 405 410 415 Ala Leu Leu Asn Lys Asp Leu Lys Pro Gln Thr Phe Arg Asn Ala Tyr 420 425 430 Asp Ile Pro Arg Arg Asn Leu Leu Asp His Leu Thr Arg Met Arg Ser 435 440 445 Asn Leu Leu Lys Ser Thr Arg Lys Phe Leu Lys Gly Gln Asp Glu Asp 450 455 460 Gln Val His Ser Val Pro Ile Ala Gln Met Gly Asn Tyr Gln Glu Tyr 465 470 475 480 Leu Lys Gln Val Pro Ser Pro Leu Arg Glu Leu Asp Pro Asp Gln Pro 485 490 495 Arg Arg Leu His Thr Phe Gly Asn Pro Phe Lys Leu Asp Lys Lys Gly 500 505 510 Met Met Ile Asp Glu Ala Asp Glu Phe Val Ala Gly Pro Gln Asn Lys 515 520 525 His Lys Arg Pro Gly Glu Pro Ser Met Gln Gly Ile Pro Lys Arg Arg 530 535 540 Arg Cys Ala Ser Pro Leu Leu Arg Gly Arg Arg Gln Ser Pro Ala Val 545 550 555 560 Asn Ser His Ile Gly Gly Lys Gly Pro Pro Ala Pro Met Thr Gln Ala 565 570 575 Gln Pro Gly Leu Ile Lys Pro Leu Pro Leu His Lys Glu Ala Thr Asn 580 585 590 Asp Ser Ile Val Asp Asp Val Val Glu Asn His Val Ala Asp Gln Leu 595 600 605 Ser Ser Asp Met Thr Pro Asn Ala Met Asp Thr Glu Phe Leu Thr Ser 610 615 620 Pro Pro Asn Leu Leu Glu Pro Ser Thr Asn His Thr Glu Ala Leu Gly 625 630 635 640 His Glu His Leu Gly Asn Asn Asp Leu Thr Val Gly Gly Phe Leu Glu 645 650 655 Asn His Glu Glu Pro Arg Asn Lys Glu Gln Ser Ala Glu Glu Asn Ile 660 665 670 Pro Ala Ser Ser Leu Asn Lys Gly Lys Lys Leu Met His Cys Arg Ser 675 680 685 His Glu Glu Val Asn Thr Glu Leu Lys Ala Gln Ile Met Lys Glu Ile 690 695 700 Arg Lys Pro Gly Arg Lys Tyr Glu Arg Ile Phe Thr Leu Leu Lys His 705 710 715 720 Val Gln Gly Ser Leu Gln Thr Arg Leu Ile Phe Leu Gln Asn Val Ile 725 730 735 Lys Glu Ala Ser Arg Phe Lys Lys Arg Met Leu Ile Glu Gln Leu Glu 740 745 750 Asn Phe Leu Asp Glu Ile His Arg Arg Ala Asn Gln Ile Asn His Ile 755 760 765 Asn Ser 770 

That which is claimed is:
 1. An isolated nucleic acid molecule encoding a DEAD-box RNA helicase, wherein the nucleic acid molecule consists of a nucleotide sequence selected from the group consisting of: (a) a nucleotide sequence that encodes a protein comprising the amino acid sequence of SEQ ID NO:2; and (b) a nucleotide sequence consisting of SEQ ID NO:1.
 2. A nucleic acid vector comprising the nucleic acid molecule of claim
 1. 3. A host cell containing the vector of claim
 2. 4. A process for producing a polypeptide comprising SEQ ID NO:2, the process comprising culturing the host cell of claim 3 under conditions sufficient for the production of said polypeptide, and recovering said polypeptide from the host cell culture.
 5. An isolated polynucleotide encoding a DEAD-box RNA helicase wherein the polynucleotide consists of the nucleotide sequence set forth in SEQ ID NO:1.
 6. A vector according to claim 2, wherein said vector is selected from the group consisting of a plasmid, virus, and bacteriophage.
 7. a vector according to claims 2, wherein said isolated nucleic acid molecule is inserted into said vector in proper orientation and correct reading frame such that the protein of SEQ ID NO:2 may be expressed by a cell transformed with said vector.
 8. A vector according to claim 7, wherein said isolated nucleic acid molecule is operatively linked to a promoter sequence.
 9. An isolated nucleic acid molecule consisting of a nucleotide sequence that is completely complementary to the nucleotide sequence of claim
 7. 